UA82881C2 - Carbonylation process using metal-tridentate ligand catalysts - Google Patents

Carbonylation process using metal-tridentate ligand catalysts Download PDF

Info

Publication number: UA82881C2
Authority: UA; Ukraine
Prior art keywords: fact; carbonylation; reaction mixture; catalyst; rhodium
Prior art date: 2003-05-14

Application number

UAA200511709A

Other languages

English (en)

Ukrainian (uk)

Inventor

John Glenn Sanly

Original Assignee

Bp Chem Int Ltd

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2003-05-14

Filing date

2004-05-05

Publication date

2008-05-26

2004-05-05 Application filed by Bp Chem Int Ltd filed Critical Bp Chem Int Ltd

2008-05-26 Publication of UA82881C2 publication Critical patent/UA82881C2/uk

Links

238000000034 method Methods 0.000 title claims abstract description 82
239000003446 ligand Substances 0.000 title claims abstract description 74
238000005810 carbonylation reaction Methods 0.000 title claims abstract description 73
230000006315 carbonylation Effects 0.000 title claims abstract description 64
239000003054 catalyst Substances 0.000 title claims abstract description 52
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 57
UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims abstract description 52
229910002091 carbon monoxide Inorganic materials 0.000 claims abstract description 51
MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 claims abstract description 48
229910052703 rhodium Inorganic materials 0.000 claims abstract description 44
239000010948 rhodium Substances 0.000 claims abstract description 44
150000001732 carboxylic acid derivatives Chemical class 0.000 claims abstract description 35
229910017052 cobalt Inorganic materials 0.000 claims abstract description 28
239000010941 cobalt Substances 0.000 claims abstract description 28
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims abstract description 28
238000004519 manufacturing process Methods 0.000 claims abstract description 6
229910052738 indium Inorganic materials 0.000 claims abstract description 4
APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 claims abstract description 4
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 105
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Natural products CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 78
239000007788 liquid Substances 0.000 claims description 71
229910052739 hydrogen Inorganic materials 0.000 claims description 59
239000001257 hydrogen Substances 0.000 claims description 59
239000011541 reaction mixture Substances 0.000 claims description 55
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 51
239000000203 mixture Substances 0.000 claims description 43
GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 claims description 34
150000002148 esters Chemical class 0.000 claims description 30
229910052751 metal Inorganic materials 0.000 claims description 29
229910052741 iridium Inorganic materials 0.000 claims description 28
150000001875 compounds Chemical class 0.000 claims description 25
229910001868 water Inorganic materials 0.000 claims description 24
239000002184 metal Substances 0.000 claims description 23
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 22
XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims description 19
KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical group [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims description 19
229910052707 ruthenium Inorganic materials 0.000 claims description 19
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims description 13
239000003426 co-catalyst Substances 0.000 claims description 13
KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 claims description 12
150000001350 alkyl halides Chemical class 0.000 claims description 12
125000000217 alkyl group Chemical group 0.000 claims description 11
150000004820 halides Chemical class 0.000 claims description 9
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 9
229910000073 phosphorus hydride Inorganic materials 0.000 claims description 9
125000003118 aryl group Chemical group 0.000 claims description 8
INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 claims description 8
229910052762 osmium Inorganic materials 0.000 claims description 6
SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical compound [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 claims description 6
229930195733 hydrocarbon Natural products 0.000 claims description 5
150000002430 hydrocarbons Chemical class 0.000 claims description 5
230000017105 transposition Effects 0.000 claims description 5
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 4
125000003342 alkenyl group Chemical group 0.000 claims description 4
229910052793 cadmium Inorganic materials 0.000 claims description 4
BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 claims description 4
TXCDCPKCNAJMEE-UHFFFAOYSA-N dibenzofuran Chemical compound C1=CC=C2C3=CC=CC=C3OC2=C1 TXCDCPKCNAJMEE-UHFFFAOYSA-N 0.000 claims description 4
150000002170 ethers Chemical class 0.000 claims description 4
229910052698 phosphorus Inorganic materials 0.000 claims description 4
238000002407 reforming Methods 0.000 claims description 4
150000003839 salts Chemical class 0.000 claims description 4
125000001424 substituent group Chemical group 0.000 claims description 4
229910052721 tungsten Inorganic materials 0.000 claims description 4
239000010937 tungsten Substances 0.000 claims description 4
CXNIUSPIQKWYAI-UHFFFAOYSA-N xantphos Chemical class C=12OC3=C(P(C=4C=CC=CC=4)C=4C=CC=CC=4)C=CC=C3C(C)(C)C2=CC=CC=1P(C=1C=CC=CC=1)C1=CC=CC=C1 CXNIUSPIQKWYAI-UHFFFAOYSA-N 0.000 claims description 4
GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 claims description 3
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 3
229910001516 alkali metal iodide Inorganic materials 0.000 claims description 3
229910001619 alkaline earth metal iodide Inorganic materials 0.000 claims description 3
125000003545 alkoxy group Chemical group 0.000 claims description 3
238000010924 continuous production Methods 0.000 claims description 3
GPAYUJZHTULNBE-UHFFFAOYSA-N diphenylphosphine Chemical compound C=1C=CC=CC=1PC1=CC=CC=C1 GPAYUJZHTULNBE-UHFFFAOYSA-N 0.000 claims description 3
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
229910052733 gallium Inorganic materials 0.000 claims description 3
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 claims description 3
229910052753 mercury Inorganic materials 0.000 claims description 3
239000011574 phosphorus Substances 0.000 claims description 3
229910052702 rhenium Inorganic materials 0.000 claims description 3
WUAPFZMCVAUBPE-UHFFFAOYSA-N rhenium atom Chemical compound [Re] WUAPFZMCVAUBPE-UHFFFAOYSA-N 0.000 claims description 3
WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 3
229910052725 zinc Inorganic materials 0.000 claims description 3
239000011701 zinc Substances 0.000 claims description 3
239000004215 Carbon black (E152) Substances 0.000 claims description 2
USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 claims description 2
HZVOZRGWRWCICA-UHFFFAOYSA-N methanediyl Chemical compound [CH2] HZVOZRGWRWCICA-UHFFFAOYSA-N 0.000 claims description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
229910052760 oxygen Inorganic materials 0.000 claims 2
125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 claims 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
239000001301 oxygen Substances 0.000 claims 1
238000012876 topography Methods 0.000 claims 1
-1 alcohol ester Chemical class 0.000 abstract description 15
239000002253 acid Substances 0.000 abstract description 4
238000006243 chemical reaction Methods 0.000 description 38
239000007789 gas Substances 0.000 description 29
239000003153 chemical reaction reagent Substances 0.000 description 27
239000000047 product Substances 0.000 description 22
238000002474 experimental method Methods 0.000 description 21
230000000052 comparative effect Effects 0.000 description 20
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 19
230000015572 biosynthetic process Effects 0.000 description 17
238000003786 synthesis reaction Methods 0.000 description 14
IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 10
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 8
125000004432 carbon atom Chemical group C* 0.000 description 8
150000002431 hydrogen Chemical class 0.000 description 8
150000001735 carboxylic acids Chemical class 0.000 description 7
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
229910052799 carbon Inorganic materials 0.000 description 6
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 6
238000002347 injection Methods 0.000 description 6
239000007924 injection Substances 0.000 description 6
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 6
150000001298 alcohols Chemical class 0.000 description 5
150000001721 carbon Chemical group 0.000 description 5
238000001816 cooling Methods 0.000 description 5
239000012263 liquid product Substances 0.000 description 5
LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 4
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
238000010521 absorption reaction Methods 0.000 description 4
229910052785 arsenic Inorganic materials 0.000 description 4
RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 4
125000004429 atom Chemical group 0.000 description 4
229910002092 carbon dioxide Inorganic materials 0.000 description 4
239000001569 carbon dioxide Substances 0.000 description 4
239000012018 catalyst precursor Substances 0.000 description 4
230000003197 catalytic effect Effects 0.000 description 4
VURFVHCLMJOLKN-UHFFFAOYSA-N diphosphane Chemical compound PP VURFVHCLMJOLKN-UHFFFAOYSA-N 0.000 description 4
238000009826 distribution Methods 0.000 description 4
238000005984 hydrogenation reaction Methods 0.000 description 4
239000007791 liquid phase Substances 0.000 description 4
HSZCZNFXUDYRKD-UHFFFAOYSA-M lithium iodide Chemical compound [Li+].[I-] HSZCZNFXUDYRKD-UHFFFAOYSA-M 0.000 description 4
238000011068 loading method Methods 0.000 description 4
150000002739 metals Chemical class 0.000 description 4
229910052757 nitrogen Inorganic materials 0.000 description 4
NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Substances [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 4
238000010926 purge Methods 0.000 description 4
239000000725 suspension Substances 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 3
239000006227 byproduct Substances 0.000 description 3
239000000539 dimer Substances 0.000 description 3
239000012535 impurity Substances 0.000 description 3
WJIBZZVTNMAURL-UHFFFAOYSA-N phosphane;rhodium Chemical compound P.[Rh] WJIBZZVTNMAURL-UHFFFAOYSA-N 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
235000019260 propionic acid Nutrition 0.000 description 3
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 3
238000000926 separation method Methods 0.000 description 3
239000011734 sodium Substances 0.000 description 3
FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 3
239000002904 solvent Substances 0.000 description 3
DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 2
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 2
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 2
150000001242 acetic acid derivatives Chemical class 0.000 description 2
238000004458 analytical method Methods 0.000 description 2
239000011575 calcium Substances 0.000 description 2
150000001733 carboxylic acid esters Chemical group 0.000 description 2
229910052804 chromium Inorganic materials 0.000 description 2
239000011651 chromium Substances 0.000 description 2
DHCWLIOIJZJFJE-UHFFFAOYSA-L dichlororuthenium Chemical compound Cl[Ru]Cl DHCWLIOIJZJFJE-UHFFFAOYSA-L 0.000 description 2
238000004821 distillation Methods 0.000 description 2
238000007429 general method Methods 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
150000004694 iodide salts Chemical class 0.000 description 2
229910052742 iron Inorganic materials 0.000 description 2
238000002955 isolation Methods 0.000 description 2
239000000463 material Substances 0.000 description 2
229910052750 molybdenum Inorganic materials 0.000 description 2
239000011733 molybdenum Substances 0.000 description 2
125000004430 oxygen atom Chemical group O* 0.000 description 2
125000004437 phosphorous atom Chemical group 0.000 description 2
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
230000002829 reductive effect Effects 0.000 description 2
150000003283 rhodium Chemical class 0.000 description 2
238000003756 stirring Methods 0.000 description 2
229910052717 sulfur Inorganic materials 0.000 description 2
229910052726 zirconium Inorganic materials 0.000 description 2
VYXHVRARDIDEHS-QGTKBVGQSA-N (1z,5z)-cycloocta-1,5-diene Chemical compound C\1C\C=C/CC\C=C/1 VYXHVRARDIDEHS-QGTKBVGQSA-N 0.000 description 1
JZKMSAGUCSIIAH-ITZCMCNPSA-N (2r)-2-amino-3-propylsulfinylpropanoic acid Chemical compound CCCS(=O)C[C@H](N)C(O)=O JZKMSAGUCSIIAH-ITZCMCNPSA-N 0.000 description 1
ZVYYAYJIGYODSD-LNTINUHCSA-K (z)-4-bis[[(z)-4-oxopent-2-en-2-yl]oxy]gallanyloxypent-3-en-2-one Chemical compound [Ga+3].C\C([O-])=C\C(C)=O.C\C([O-])=C\C(C)=O.C\C([O-])=C\C(C)=O ZVYYAYJIGYODSD-LNTINUHCSA-K 0.000 description 1
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ANOOTOPTCJRUPK-UHFFFAOYSA-N 1-iodohexane Chemical compound CCCCCCI ANOOTOPTCJRUPK-UHFFFAOYSA-N 0.000 description 1
229940101798 4-cymene Drugs 0.000 description 1
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
UNMYWSMUMWPJLR-UHFFFAOYSA-L Calcium iodide Chemical compound [Ca+2].[I-].[I-] UNMYWSMUMWPJLR-UHFFFAOYSA-L 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
229910052684 Cerium Inorganic materials 0.000 description 1
229910019001 CoSi Inorganic materials 0.000 description 1
241000276573 Cottidae Species 0.000 description 1
206010072268 Drug-induced liver injury Diseases 0.000 description 1
241000282326 Felis catus Species 0.000 description 1
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241000286819 Malo Species 0.000 description 1
JOLPMNSROALHES-UHFFFAOYSA-L O.O.O.[Ru](Cl)Cl Chemical compound O.O.O.[Ru](Cl)Cl JOLPMNSROALHES-UHFFFAOYSA-L 0.000 description 1
108091034117 Oligonucleotide Proteins 0.000 description 1
101150024701 PPH3 gene Proteins 0.000 description 1
229910052772 Samarium Inorganic materials 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
XJUCCGJZENLZSA-UHFFFAOYSA-M [Rh]Cl Chemical compound [Rh]Cl XJUCCGJZENLZSA-UHFFFAOYSA-M 0.000 description 1
ROZSPJBPUVWBHW-UHFFFAOYSA-N [Ru]=O Chemical class [Ru]=O ROZSPJBPUVWBHW-UHFFFAOYSA-N 0.000 description 1
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150000004729 acetoacetic acid derivatives Chemical class 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
150000001299 aldehydes Chemical class 0.000 description 1
150000001351 alkyl iodides Chemical class 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
125000000732 arylene group Chemical group 0.000 description 1
238000002453 autothermal reforming Methods 0.000 description 1
238000010923 batch production Methods 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
VNBCLZZFHLADIG-UHFFFAOYSA-K butanoate ruthenium(3+) Chemical compound [Ru+3].CCCC([O-])=O.CCCC([O-])=O.CCCC([O-])=O VNBCLZZFHLADIG-UHFFFAOYSA-K 0.000 description 1
229910001640 calcium iodide Inorganic materials 0.000 description 1
229940046413 calcium iodide Drugs 0.000 description 1
GGRQQHADVSXBQN-FGSKAQBVSA-N carbon monoxide;(z)-4-hydroxypent-3-en-2-one;rhodium Chemical compound [Rh].[O+]#[C-].[O+]#[C-].C\C(O)=C\C(C)=O GGRQQHADVSXBQN-FGSKAQBVSA-N 0.000 description 1
NQZFAUXPNWSLBI-UHFFFAOYSA-N carbon monoxide;ruthenium Chemical group [Ru].[Ru].[Ru].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-] NQZFAUXPNWSLBI-UHFFFAOYSA-N 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
ZMIGMASIKSOYAM-UHFFFAOYSA-N cerium Chemical compound [Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce] ZMIGMASIKSOYAM-UHFFFAOYSA-N 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
JIXOCHSERUXVMW-UHFFFAOYSA-M chlororuthenium Chemical compound [Ru]Cl JIXOCHSERUXVMW-UHFFFAOYSA-M 0.000 description 1
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238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
239000004035 construction material Substances 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
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229910052906 cristobalite Inorganic materials 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
238000011161 development Methods 0.000 description 1
FYWVTSQYJIPZLW-UHFFFAOYSA-K diacetyloxygallanyl acetate Chemical compound [Ga+3].CC([O-])=O.CC([O-])=O.CC([O-])=O FYWVTSQYJIPZLW-UHFFFAOYSA-K 0.000 description 1
VBXWCGWXDOBUQZ-UHFFFAOYSA-K diacetyloxyindiganyl acetate Chemical compound [In+3].CC([O-])=O.CC([O-])=O.CC([O-])=O VBXWCGWXDOBUQZ-UHFFFAOYSA-K 0.000 description 1
150000001983 dialkylethers Chemical group 0.000 description 1
ZPFKAZDQKQTOIW-UHFFFAOYSA-L dibromorhodium Chemical compound Br[Rh]Br ZPFKAZDQKQTOIW-UHFFFAOYSA-L 0.000 description 1
HBIHVBJJZAHVLE-UHFFFAOYSA-L dibromoruthenium Chemical compound Br[Ru]Br HBIHVBJJZAHVLE-UHFFFAOYSA-L 0.000 description 1
125000003963 dichloro group Chemical group Cl* 0.000 description 1
OAGAGESCFZXSJR-UHFFFAOYSA-L dichloroosmium Chemical compound Cl[Os]Cl OAGAGESCFZXSJR-UHFFFAOYSA-L 0.000 description 1
NKDDWNXOKDWJAK-UHFFFAOYSA-N dimethoxymethane Chemical compound COCOC NKDDWNXOKDWJAK-UHFFFAOYSA-N 0.000 description 1
POLCUAVZOMRGSN-UHFFFAOYSA-N dipropyl ether Chemical compound CCCOCCC POLCUAVZOMRGSN-UHFFFAOYSA-N 0.000 description 1
230000000694 effects Effects 0.000 description 1
238000005886 esterification reaction Methods 0.000 description 1
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238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
238000000605 extraction Methods 0.000 description 1
238000004508 fractional distillation Methods 0.000 description 1
UIWYJDYFSGRHKR-UHFFFAOYSA-N gadolinium atom Chemical compound [Gd] UIWYJDYFSGRHKR-UHFFFAOYSA-N 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
150000004687 hexahydrates Chemical class 0.000 description 1
238000011905 homologation Methods 0.000 description 1
DKAGJZJALZXOOV-UHFFFAOYSA-N hydrate;hydrochloride Chemical compound O.Cl DKAGJZJALZXOOV-UHFFFAOYSA-N 0.000 description 1
125000001183 hydrocarbyl group Chemical group 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
238000011065 in-situ storage Methods 0.000 description 1
SKWCWFYBFZIXHE-UHFFFAOYSA-K indium acetylacetonate Chemical compound CC(=O)C=C(C)O[In](OC(C)=CC(C)=O)OC(C)=CC(C)=O SKWCWFYBFZIXHE-UHFFFAOYSA-K 0.000 description 1
HVTICUPFWKNHNG-UHFFFAOYSA-N iodoethane Chemical compound CCI HVTICUPFWKNHNG-UHFFFAOYSA-N 0.000 description 1
239000003456 ion exchange resin Substances 0.000 description 1
229920003303 ion-exchange polymer Polymers 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
150000002503 iridium Chemical class 0.000 description 1
KZLHPYLCKHJIMM-UHFFFAOYSA-K iridium(3+);triacetate Chemical compound [Ir+3].CC([O-])=O.CC([O-])=O.CC([O-])=O KZLHPYLCKHJIMM-UHFFFAOYSA-K 0.000 description 1
229910052747 lanthanoid Inorganic materials 0.000 description 1
150000002602 lanthanoids Chemical class 0.000 description 1
239000012528 membrane Substances 0.000 description 1
238000002156 mixing Methods 0.000 description 1
PVWOIHVRPOBWPI-UHFFFAOYSA-N n-propyl iodide Chemical compound CCCI PVWOIHVRPOBWPI-UHFFFAOYSA-N 0.000 description 1
229910052759 nickel Inorganic materials 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
229910052756 noble gas Inorganic materials 0.000 description 1
150000002835 noble gases Chemical class 0.000 description 1
229910000489 osmium tetroxide Inorganic materials 0.000 description 1
239000012285 osmium tetroxide Substances 0.000 description 1
150000003901 oxalic acid esters Chemical class 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
HFPZCAJZSCWRBC-UHFFFAOYSA-N p-cymene Natural products CC(C)C1=CC=C(C)C=C1 HFPZCAJZSCWRBC-UHFFFAOYSA-N 0.000 description 1
LSMAIBOZUPTNBR-UHFFFAOYSA-N phosphanium;iodide Chemical class [PH4+].[I-] LSMAIBOZUPTNBR-UHFFFAOYSA-N 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
239000002243 precursor Substances 0.000 description 1
238000012545 processing Methods 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000001453 quaternary ammonium group Chemical group 0.000 description 1
SVOOVMQUISJERI-UHFFFAOYSA-K rhodium(3+);triacetate Chemical compound [Rh+3].CC([O-])=O.CC([O-])=O.CC([O-])=O SVOOVMQUISJERI-UHFFFAOYSA-K 0.000 description 1
KXAHUXSHRWNTOD-UHFFFAOYSA-K rhodium(3+);triiodide Chemical compound [Rh+3].[I-].[I-].[I-] KXAHUXSHRWNTOD-UHFFFAOYSA-K 0.000 description 1
229910001925 ruthenium oxide Inorganic materials 0.000 description 1
YAYGSLOSTXKUBW-UHFFFAOYSA-N ruthenium(2+) Chemical compound [Ru+2] YAYGSLOSTXKUBW-UHFFFAOYSA-N 0.000 description 1
BNBKCTCLPAQLAH-UHFFFAOYSA-K ruthenium(3+) triformate Chemical compound [Ru+3].[O-]C=O.[O-]C=O.[O-]C=O BNBKCTCLPAQLAH-UHFFFAOYSA-K 0.000 description 1
OJLCQGGSMYKWEK-UHFFFAOYSA-K ruthenium(3+);triacetate Chemical compound [Ru+3].CC([O-])=O.CC([O-])=O.CC([O-])=O OJLCQGGSMYKWEK-UHFFFAOYSA-K 0.000 description 1
KZUNJOHGWZRPMI-UHFFFAOYSA-N samarium atom Chemical compound [Sm] KZUNJOHGWZRPMI-UHFFFAOYSA-N 0.000 description 1
238000005070 sampling Methods 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
235000009518 sodium iodide Nutrition 0.000 description 1
239000000243 solution Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
238000000629 steam reforming Methods 0.000 description 1
229910052682 stishovite Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
125000004434 sulfur atom Chemical group 0.000 description 1
238000012360 testing method Methods 0.000 description 1
150000004685 tetrahydrates Chemical class 0.000 description 1
229910052905 tridymite Inorganic materials 0.000 description 1
238000009423 ventilation Methods 0.000 description 1
238000002424 x-ray crystallography Methods 0.000 description 1
NHXVNEDMKGDNPR-UHFFFAOYSA-N zinc;pentane-2,4-dione Chemical compound [Zn+2].CC(=O)[CH-]C(C)=O.CC(=O)[CH-]C(C)=O NHXVNEDMKGDNPR-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/36—Preparation of carboxylic acid esters by reaction with carbon monoxide or formates
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/10—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide
- C07C51/12—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide on an oxygen-containing group in organic compounds, e.g. alcohols
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C53/00—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen
- C07C53/08—Acetic acid

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Engineering & Computer Science (AREA)
Oil, Petroleum & Natural Gas (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Catalysts (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Glass Compositions (AREA)
Iron Core Of Rotating Electric Machines (AREA)

UAA200511709A 2003-05-14 2004-05-05 Carbonylation process using metal-tridentate ligand catalysts UA82881C2 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
GBGB0311091.3A GB0311091D0 (en)	2003-05-14	2003-05-14	Process
PCT/GB2004/001943 WO2004101488A1 (en)	2003-05-14	2004-05-05	Carbonylation process using metal-tridentate ligand catalysts

Publications (1)

Publication Number	Publication Date
UA82881C2 true UA82881C2 (en)	2008-05-26

Family

ID=9958065

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
UAA200511709A UA82881C2 (en)	2003-05-14	2004-05-05	Carbonylation process using metal-tridentate ligand catalysts

Country Status (18)

Country	Link
US (1)	US7276626B2 (de)
EP (1)	EP1622854B1 (de)
JP (2)	JP5336702B2 (de)
KR (1)	KR101051905B1 (de)
CN (1)	CN1823029B (de)
AT (1)	ATE392409T1 (de)
BR (1)	BRPI0410217B1 (de)
CA (1)	CA2525025C (de)
DE (1)	DE602004013137T2 (de)
ES (1)	ES2303072T3 (de)
GB (1)	GB0311091D0 (de)
MY (1)	MY137682A (de)
NO (1)	NO20055949L (de)
RS (1)	RS52828B (de)
RU (1)	RU2348607C2 (de)
TW (1)	TWI355376B (de)
UA (1)	UA82881C2 (de)
WO (1)	WO2004101488A1 (de)

Families Citing this family (16)

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US7053241B1 (en)	2005-02-24	2006-05-30	Celanese International Corporation	Acetic acid production methods incorporating at least one metal salt as a catalyst stabilizer
GB0601865D0 (en) *	2006-01-30	2006-03-08	Bp Chem Int Ltd	Process
TWI473785B (zh) *	2007-06-01	2015-02-21	Bp Chem Int Ltd	使用金屬螯配位體催化劑用於醋酸之生產的羰基化方法
US7608744B1 (en)	2008-07-31	2009-10-27	Celanese International Corporation	Ethanol production from acetic acid utilizing a cobalt catalyst
US7884253B2 (en) *	2008-12-11	2011-02-08	Range Fuels, Inc.	Methods and apparatus for selectively producing ethanol from synthesis gas
US8785684B2 (en)	2010-06-14	2014-07-22	Celanese International Corporation	Methanol carbonylation process with rhodium catalyst, an iodide salt and a metallic co-catalyst selected from transition metals, indium, strontium, barium, zinc, tin and heteropoly acids
WO2011159268A1 (en)	2010-06-14	2011-12-22	Celanese Internaltional Corporation	Carbonylation process
US8835681B2 (en)	2010-06-14	2014-09-16	Celanese International Corporation	Methanol carbonylation process with rhodium catalyst and a lanthanide metal co-catalyst
SG11201705237XA (en)	2015-01-20	2017-07-28	Lyondellbasell Acetyls Llc	Use of a ruthenium promoter in a phosphine oxide carbonylation process
US9822055B2 (en)	2015-06-23	2017-11-21	Lyondellbasell Acetyls, Llc	Silver loaded halide removal resins for treating halide containing solutions
CN106748772B (zh) *	2016-11-29	2019-05-07	西南化工研究设计院有限公司	一种醋酸甲酯的生产方法
CN111111774A (zh) *	2018-11-01	2020-05-08	中国科学院大连化学物理研究所	有机含膦聚合物载体负载铑和杂多酸催化剂及制备和应用
US11365171B2 (en) *	2019-06-12	2022-06-21	Evonik Operations Gmbh	Process for preparing an ester by alkoxycarbonylation
CN113788748A (zh) *	2021-09-15	2021-12-14	华东师范大学	多齿膦配体修饰的钯组合催化剂催化不饱和烃制备直链羰基化合物的方法
CN113877635B (zh) *	2021-10-27	2024-02-06	南京延长反应技术研究院有限公司	一种铱基催化剂及其制备方法、醛化方法
US20250074856A1 (en) *	2023-08-31	2025-03-06	Lyondellbasell Acetyls, Llc	Polyphoshates and polyphosphonates as rate promoters for the glacial acetic acid process

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US4321211A (en) *	1971-07-27	1982-03-23	Exxon Research & Engineering Co.	Carbonylation catalysts
US4102920A (en) *	1977-01-13	1978-07-25	Air Products & Chemicals, Inc.	Production of carboxylic acids and esters
US4102921A (en)	1977-04-26	1978-07-25	Air Products & Chemicals, Inc.	Production of carboxylic acids and esters
JPH06503808A (ja) *	1990-08-31	1994-04-28	ザ　ガヴァナーズ　オヴ　ザ　ユニヴァーシティ　オヴ　アルバータ	新規の遷移金属触媒先駆物質を用いるメタノールのカルボニル化
GB2336154B (en) *	1998-04-07	2003-04-16	Bp Chem Int Ltd	Process for carbonylation of an alcohol and/or reactive derivative thereof
GB9825424D0 (en) *	1998-11-19	1999-01-13	Bp Chem Int Ltd	Process
ES2258431T3 (es) *	1999-08-02	2006-09-01	F. Hoffmann-La Roche Ag	Proceso para la preparacion de derivados de benzotiofeno.
GB9926854D0 (en) *	1999-11-12	2000-01-12	Bp Chem Int Ltd	Process
IT1318653B1 (it) *	2000-07-28	2003-08-27	Enichem Spa	Leganti tridentati e loro complessi con metalli di transizione.
GB0311092D0 (en) *	2003-05-14	2003-06-18	Bp Chem Int Ltd	Process

2003
- 2003-05-14 GB GBGB0311091.3A patent/GB0311091D0/en not_active Ceased
2004
- 2004-05-05 KR KR1020057021417A patent/KR101051905B1/ko not_active Expired - Fee Related
- 2004-05-05 AT AT04731209T patent/ATE392409T1/de not_active IP Right Cessation
- 2004-05-05 RU RU2005138786/04A patent/RU2348607C2/ru not_active IP Right Cessation
- 2004-05-05 ES ES04731209T patent/ES2303072T3/es not_active Expired - Lifetime
- 2004-05-05 UA UAA200511709A patent/UA82881C2/uk unknown
- 2004-05-05 RS YU20050846A patent/RS52828B/sr unknown
- 2004-05-05 DE DE602004013137T patent/DE602004013137T2/de not_active Expired - Lifetime
- 2004-05-05 JP JP2006530477A patent/JP5336702B2/ja not_active Expired - Fee Related
- 2004-05-05 US US10/555,417 patent/US7276626B2/en not_active Expired - Fee Related
- 2004-05-05 EP EP04731209A patent/EP1622854B1/de not_active Expired - Lifetime
- 2004-05-05 WO PCT/GB2004/001943 patent/WO2004101488A1/en not_active Ceased
- 2004-05-05 CN CN2004800198286A patent/CN1823029B/zh not_active Expired - Fee Related
- 2004-05-05 BR BRPI0410217-7B1A patent/BRPI0410217B1/pt not_active IP Right Cessation
- 2004-05-05 CA CA2525025A patent/CA2525025C/en not_active Expired - Fee Related
- 2004-05-13 MY MYPI20041791A patent/MY137682A/en unknown
- 2004-05-13 TW TW093113467A patent/TWI355376B/zh not_active IP Right Cessation
2005
- 2005-12-14 NO NO20055949A patent/NO20055949L/no unknown
2011
- 2011-08-13 JP JP2011177358A patent/JP2012006957A/ja not_active Withdrawn

Also Published As

Publication number	Publication date
NO20055949L (no)	2005-12-14
EP1622854A1 (de)	2006-02-08
DE602004013137T2 (de)	2009-07-02
US7276626B2 (en)	2007-10-02
MY137682A (en)	2009-02-27
RU2348607C2 (ru)	2009-03-10
KR20060006963A (ko)	2006-01-20
RU2005138786A (ru)	2007-06-27
CN1823029A (zh)	2006-08-23
KR101051905B1 (ko)	2011-07-26
EP1622854B1 (de)	2008-04-16
GB0311091D0 (en)	2003-06-18
JP2012006957A (ja)	2012-01-12
CA2525025C (en)	2012-07-10
ATE392409T1 (de)	2008-05-15
JP5336702B2 (ja)	2013-11-06
JP2006528960A (ja)	2006-12-28
RS52828B (sr)	2013-10-31
DE602004013137D1 (de)	2008-05-29
BRPI0410217A (pt)	2006-05-09
TW200500332A (en)	2005-01-01
CA2525025A1 (en)	2004-11-25
WO2004101488A1 (en)	2004-11-25
CN1823029B (zh)	2010-09-29
RS20050846A (sr)	2008-04-04
ES2303072T3 (es)	2008-08-01
TWI355376B (en)	2012-01-01
BRPI0410217B1 (pt)	2013-09-03
US20060173212A1 (en)	2006-08-03

Publication	Publication Date	Title
CA2225142C (en)	2006-12-05	Iridium-catalysed carbonylation process for the production of acetic acid
EP0846674B1 (de)	2001-01-10	Iridium katalysiertes Carbonylierungsverfahren zur Herstellung einer Carbonsäure
UA82881C2 (en)	2008-05-26	Carbonylation process using metal-tridentate ligand catalysts
TW528748B (en)	2003-04-21	Process for the production of acetic acid
CA2524981C (en)	2011-12-20	Carbonylation process using metal-polydentate ligand catalysts
JP3766437B2 (ja)	2006-04-12	イリジウム存在下のカルボニル化によるカルボン酸類又はそのエステル類の製造
CA2348472C (en)	2009-03-31	Method for preparing acetic acid and/or methyl acetate in the presence of iridium and platinum
JPS6346735B2 (de)	1988-09-19
US4661623A (en)	1987-04-28	Method of producing methyl formate from methanol and carbon monoxide using anionic group VIII metal cataysts
EP0999198A1 (de)	2000-05-10	Verfahren zur Herstellung von Essigsäure
CA2637325C (en)	2013-04-23	Process for the production of acetic acid
WO2007085792A1 (en)	2007-08-02	Process for the production of acetic acid
JPH0145A (ja)	1989-01-05	２−クロロプロピオンアルデヒドの製造方法
JPS6372643A (ja)	1988-04-02	２−クロロプロピオンアルデヒドの製造方法
JPS5867641A (ja)	1983-04-22	酢酸の合成方法