LU85703A1 - Procede de preparation de phenols halogenes - Google Patents

Procede de preparation de phenols halogenes Download PDF

Info

Publication number: LU85703A1
Authority: LU; Luxembourg
Prior art keywords: group; free; modified; organic functional; groups
Prior art date: 1983-12-21

Application number

LU85703A

Other languages

English (en)

French (fr)

Inventor

Aurelio Romeo

Francesco Della Valle

Original Assignee

Fidia Spa

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.)

1983-12-21

Filing date

1984-12-20

Publication date

1985-07-24

1984-12-20 Application filed by Fidia Spa filed Critical Fidia Spa

1985-07-24 Publication of LU85703A1 publication Critical patent/LU85703A1/fr

Links

238000000034 method Methods 0.000 title claims description 51
230000008569 process Effects 0.000 title claims description 20
238000002360 preparation method Methods 0.000 title claims description 16
150000002989 phenols Chemical class 0.000 title description 3
125000000524 functional group Chemical group 0.000 claims description 39
150000003839 salts Chemical class 0.000 claims description 27
GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims description 26
239000000203 mixture Substances 0.000 claims description 25
238000006277 sulfonation reaction Methods 0.000 claims description 22
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 21
LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 claims description 20
239000000460 chlorine Substances 0.000 claims description 19
229910052801 chlorine Inorganic materials 0.000 claims description 19
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 18
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 17
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 16
229910052736 halogen Chemical class 0.000 claims description 15
238000005658 halogenation reaction Methods 0.000 claims description 14
150000002367 halogens Chemical class 0.000 claims description 14
ZZJVDYQPZOHNIK-UHFFFAOYSA-N 2,6-dihydroxybenzenesulfonic acid Chemical compound OC1=CC=CC(O)=C1S(O)(=O)=O ZZJVDYQPZOHNIK-UHFFFAOYSA-N 0.000 claims description 13
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 13
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 12
229910052794 bromium Inorganic materials 0.000 claims description 12
238000005660 chlorination reaction Methods 0.000 claims description 12
125000004432 carbon atom Chemical group C* 0.000 claims description 11
150000002148 esters Chemical class 0.000 claims description 11
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 11
238000005893 bromination reaction Methods 0.000 claims description 9
230000026030 halogenation Effects 0.000 claims description 8
150000002170 ethers Chemical class 0.000 claims description 7
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 6
125000003277 amino group Chemical class 0.000 claims description 6
230000031709 bromination Effects 0.000 claims description 6
125000005843 halogen group Chemical group 0.000 claims description 6
230000002140 halogenating effect Effects 0.000 claims description 6
238000011065 in-situ storage Methods 0.000 claims description 6
239000011630 iodine Substances 0.000 claims description 6
229910052740 iodine Inorganic materials 0.000 claims description 6
150000007524 organic acids Chemical class 0.000 claims description 5
125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 claims description 5
125000001424 substituent group Chemical group 0.000 claims description 5
150000001412 amines Chemical class 0.000 claims description 3
230000009466 transformation Effects 0.000 claims description 3
150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 2
230000008030 elimination Effects 0.000 claims description 2
238000003379 elimination reaction Methods 0.000 claims description 2
150000002430 hydrocarbons Chemical group 0.000 claims 4
WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-Phenylethanol Natural products OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 claims 3
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims 2
230000026045 iodination Effects 0.000 claims 2
238000006192 iodination reaction Methods 0.000 claims 2
DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
229940067107 phenylethyl alcohol Drugs 0.000 claims 1
125000001302 tertiary amino group Chemical group 0.000 claims 1
239000002253 acid Substances 0.000 description 31
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 24
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 22
150000007513 acids Chemical class 0.000 description 20
SWZVJOLLQTWFCW-UHFFFAOYSA-N 2-chlorobenzene-1,3-diol Chemical compound OC1=CC=CC(O)=C1Cl SWZVJOLLQTWFCW-UHFFFAOYSA-N 0.000 description 17
-1 aliphatic alcohols Chemical class 0.000 description 16
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 15
239000000243 solution Substances 0.000 description 13
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 12
239000007864 aqueous solution Substances 0.000 description 12
229960001755 resorcinol Drugs 0.000 description 12
125000001183 hydrocarbyl group Chemical group 0.000 description 11
238000006243 chemical reaction Methods 0.000 description 10
239000011541 reaction mixture Substances 0.000 description 10
XTEGARKTQYYJKE-UHFFFAOYSA-M Chlorate Chemical class [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 description 9
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
238000000926 separation method Methods 0.000 description 9
150000001875 compounds Chemical class 0.000 description 8
239000000047 product Substances 0.000 description 8
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 6
125000001931 aliphatic group Chemical group 0.000 description 6
238000000605 extraction Methods 0.000 description 6
239000012429 reaction media Substances 0.000 description 6
SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 5
238000005903 acid hydrolysis reaction Methods 0.000 description 5
229910052783 alkali metal Inorganic materials 0.000 description 5
239000008346 aqueous phase Substances 0.000 description 5
229910052739 hydrogen Inorganic materials 0.000 description 5
239000000543 intermediate Substances 0.000 description 5
150000003460 sulfonic acids Chemical class 0.000 description 5
150000005207 1,3-dihydroxybenzenes Chemical class 0.000 description 4
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
230000002378 acidificating effect Effects 0.000 description 4
150000001340 alkali metals Chemical class 0.000 description 4
125000003118 aryl group Chemical group 0.000 description 4
238000002425 crystallisation Methods 0.000 description 4
230000008025 crystallization Effects 0.000 description 4
159000000011 group IA salts Chemical class 0.000 description 4
239000001257 hydrogen Substances 0.000 description 4
PHTQWCKDNZKARW-UHFFFAOYSA-N isoamylol Chemical compound CC(C)CCO PHTQWCKDNZKARW-UHFFFAOYSA-N 0.000 description 4
238000002844 melting Methods 0.000 description 4
230000008018 melting Effects 0.000 description 4
235000005985 organic acids Nutrition 0.000 description 4
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 4
238000010992 reflux Methods 0.000 description 4
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 4
DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
125000004423 acyloxy group Chemical group 0.000 description 3
239000003513 alkali Substances 0.000 description 3
229910052784 alkaline earth metal Inorganic materials 0.000 description 3
125000000217 alkyl group Chemical group 0.000 description 3
125000003368 amide group Chemical group 0.000 description 3
238000004458 analytical method Methods 0.000 description 3
230000015572 biosynthetic process Effects 0.000 description 3
SXDBWCPKPHAZSM-UHFFFAOYSA-M bromate Chemical class [O-]Br(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-M 0.000 description 3
239000003153 chemical reaction reagent Substances 0.000 description 3
239000003085 diluting agent Substances 0.000 description 3
238000001704 evaporation Methods 0.000 description 3
230000008020 evaporation Effects 0.000 description 3
229910052731 fluorine Inorganic materials 0.000 description 3
239000011737 fluorine Substances 0.000 description 3
FUZZWVXGSFPDMH-UHFFFAOYSA-M hexanoate Chemical compound CCCCCC([O-])=O FUZZWVXGSFPDMH-UHFFFAOYSA-M 0.000 description 3
230000004048 modification Effects 0.000 description 3
238000012986 modification Methods 0.000 description 3
230000007935 neutral effect Effects 0.000 description 3
229910052700 potassium Inorganic materials 0.000 description 3
239000011591 potassium Substances 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
239000011734 sodium Substances 0.000 description 3
238000004809 thin layer chromatography Methods 0.000 description 3
VWXVJYKCCPSYRD-UHFFFAOYSA-N 4,6-dihydroxybenzene-1,3-disulfonic acid Chemical group OC1=CC(O)=C(S(O)(=O)=O)C=C1S(O)(=O)=O VWXVJYKCCPSYRD-UHFFFAOYSA-N 0.000 description 2
IAKDZGDUVPOFBV-UHFFFAOYSA-N 5-chloro-4,6-dihydroxybenzene-1,3-disulfonic acid Chemical compound OC1=C(Cl)C(O)=C(S(O)(=O)=O)C=C1S(O)(=O)=O IAKDZGDUVPOFBV-UHFFFAOYSA-N 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
238000005904 alkaline hydrolysis reaction Methods 0.000 description 2
239000011260 aqueous acid Substances 0.000 description 2
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
235000019445 benzyl alcohol Nutrition 0.000 description 2
SXDBWCPKPHAZSM-UHFFFAOYSA-N bromic acid Chemical compound OBr(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-N 0.000 description 2
239000011575 calcium Substances 0.000 description 2
229910052791 calcium Inorganic materials 0.000 description 2
239000001913 cellulose Substances 0.000 description 2
229920002678 cellulose Polymers 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 2
238000004587 chromatography analysis Methods 0.000 description 2
125000000753 cycloalkyl group Chemical group 0.000 description 2
238000007865 diluting Methods 0.000 description 2
239000003480 eluent Substances 0.000 description 2
229910052500 inorganic mineral Inorganic materials 0.000 description 2
NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
229910052751 metal Inorganic materials 0.000 description 2
239000002184 metal Substances 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
239000011707 mineral Substances 0.000 description 2
239000012074 organic phase Substances 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 2
238000001556 precipitation Methods 0.000 description 2
238000000746 purification Methods 0.000 description 2
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
238000006479 redox reaction Methods 0.000 description 2
159000000000 sodium salts Chemical class 0.000 description 2
239000007858 starting material Substances 0.000 description 2
238000003756 stirring Methods 0.000 description 2
KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
235000011149 sulphuric acid Nutrition 0.000 description 2
239000000725 suspension Substances 0.000 description 2
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
BLIQUJLAJXRXSG-UHFFFAOYSA-N 1-benzyl-3-(trifluoromethyl)pyrrolidin-1-ium-3-carboxylate Chemical compound C1C(C(=O)O)(C(F)(F)F)CCN1CC1=CC=CC=C1 BLIQUJLAJXRXSG-UHFFFAOYSA-N 0.000 description 1
GQTHXQVZAKGYGN-UHFFFAOYSA-N 2,4-dihydroxybenzene-1,3-disulfonic acid Chemical compound OC1=CC=C(S(O)(=O)=O)C(O)=C1S(O)(=O)=O GQTHXQVZAKGYGN-UHFFFAOYSA-N 0.000 description 1
UOLPZAPIFFZLMF-UHFFFAOYSA-N 2-bromobenzene-1,3-diol Chemical compound OC1=CC=CC(O)=C1Br UOLPZAPIFFZLMF-UHFFFAOYSA-N 0.000 description 1
BMNAUVHUXKPMOO-UHFFFAOYSA-N 3,5-dihydroxybenzene-1,2,4-trisulfonic acid Chemical compound OC1=CC(S(O)(=O)=O)=C(S(O)(=O)=O)C(O)=C1S(O)(=O)=O BMNAUVHUXKPMOO-UHFFFAOYSA-N 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
239000005711 Benzoic acid Substances 0.000 description 1
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical class CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 1
KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 1
GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
IOVCWXUNBOPUCH-UHFFFAOYSA-N Nitrous acid Chemical compound ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
230000009471 action Effects 0.000 description 1
125000002252 acyl group Chemical group 0.000 description 1
150000001299 aldehydes Chemical class 0.000 description 1
125000002723 alicyclic group Chemical group 0.000 description 1
229910001854 alkali hydroxide Inorganic materials 0.000 description 1
150000008044 alkali metal hydroxides Chemical class 0.000 description 1
150000001342 alkaline earth metals Chemical class 0.000 description 1
125000005907 alkyl ester group Chemical group 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
159000000032 aromatic acids Chemical class 0.000 description 1
150000001491 aromatic compounds Chemical class 0.000 description 1
125000002029 aromatic hydrocarbon group Chemical group 0.000 description 1
235000010233 benzoic acid Nutrition 0.000 description 1
FNXLCIKXHOPCKH-UHFFFAOYSA-N bromamine Chemical class BrN FNXLCIKXHOPCKH-UHFFFAOYSA-N 0.000 description 1
150000001649 bromium compounds Chemical class 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
238000005119 centrifugation Methods 0.000 description 1
150000001805 chlorine compounds Chemical class 0.000 description 1
229940106681 chloroacetic acid Drugs 0.000 description 1
239000000470 constituent Substances 0.000 description 1
150000004775 coumarins Chemical class 0.000 description 1
239000013078 crystal Substances 0.000 description 1
239000012954 diazonium Substances 0.000 description 1
150000001989 diazonium salts Chemical class 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
150000002012 dioxanes Chemical class 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000001914 filtration Methods 0.000 description 1
238000003682 fluorination reaction Methods 0.000 description 1
235000019253 formic acid Nutrition 0.000 description 1
150000004674 formic acids Chemical class 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
230000003301 hydrolyzing effect Effects 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
150000004679 hydroxides Chemical class 0.000 description 1
150000003949 imides Chemical class 0.000 description 1
239000013067 intermediate product Substances 0.000 description 1
ICIWUVCWSCSTAQ-UHFFFAOYSA-N iodic acid Chemical class OI(=O)=O ICIWUVCWSCSTAQ-UHFFFAOYSA-N 0.000 description 1
150000004694 iodide salts Chemical class 0.000 description 1
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
238000002955 isolation Methods 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
125000002950 monocyclic group Chemical group 0.000 description 1
125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
229910017604 nitric acid Inorganic materials 0.000 description 1
239000012457 nonaqueous media Substances 0.000 description 1
125000000962 organic group Chemical group 0.000 description 1
239000007800 oxidant agent Substances 0.000 description 1
XHFXMNZYIKFCPN-UHFFFAOYSA-N perchloryl fluoride Chemical compound FCl(=O)(=O)=O XHFXMNZYIKFCPN-UHFFFAOYSA-N 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
VKJKEPKFPUWCAS-UHFFFAOYSA-M potassium chlorate Chemical compound [K+].[O-]Cl(=O)=O VKJKEPKFPUWCAS-UHFFFAOYSA-M 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
238000005932 reductive alkylation reaction Methods 0.000 description 1
230000002829 reductive effect Effects 0.000 description 1
238000006894 reductive elimination reaction Methods 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000001384 succinic acid Substances 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
NBNBICNWNFQDDD-UHFFFAOYSA-N sulfuryl dibromide Chemical compound BrS(Br)(=O)=O NBNBICNWNFQDDD-UHFFFAOYSA-N 0.000 description 1
YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 1
238000005292 vacuum distillation Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C35/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring
- C07C35/02—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring monocyclic
- C07C35/08—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring monocyclic containing a six-membered rings
- C07C35/14—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring monocyclic containing a six-membered rings with more than one hydroxy group bound to the ring
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
- C07C37/62—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by introduction of halogen; by substitution of halogen atoms by other halogen atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring

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Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

LU85703A 1983-12-21 1984-12-20 Procede de preparation de phenols halogenes LU85703A1 (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
IT8349556A IT1212907B (it)	1983-12-21	1983-12-21	Preparazione di fenoli alogenati
IT4955683		1983-12-21

Publications (1)

Publication Number	Publication Date
LU85703A1 true LU85703A1 (fr)	1985-07-24

Family

ID=11271015

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
LU85703A LU85703A1 (fr)	1983-12-21	1984-12-20	Procede de preparation de phenols halogenes

Country Status (29)

Country	Link
US (1)	US4704469A (de)
EP (1)	EP0146923B1 (de)
JP (2)	JPH0635408B2 (de)
KR (1)	KR880000202B1 (de)
AR (1)	AR240908A1 (de)
AT (1)	ATE65076T1 (de)
AU (2)	AU3711784A (de)
BE (1)	BE901323A (de)
BR (1)	BR8406649A (de)
CA (1)	CA1325812C (de)
CH (1)	CH666257A5 (de)
DE (1)	DE3484792D1 (de)
DK (1)	DK625284A (de)
ES (1)	ES8604845A1 (de)
FI (1)	FI84907C (de)
FR (1)	FR2557096B1 (de)
GR (1)	GR82532B (de)
HU (1)	HU196938B (de)
IE (1)	IE57964B1 (de)
IL (1)	IL73787A (de)
IN (1)	IN163437B (de)
IT (1)	IT1212907B (de)
LU (1)	LU85703A1 (de)
MX (1)	MX162546A (de)
NO (1)	NO164235C (de)
NZ (1)	NZ210605A (de)
PT (1)	PT79716A (de)
YU (1)	YU44992B (de)
ZA (1)	ZA849669B (de)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5410083A (en) *	1993-10-15	1995-04-25	The Dow Chemical Company	Synthesis of diaminoresorcinal from resorcinol
US5371291A (en) *	1993-10-15	1994-12-06	The Dow Chemical Company	Synthesis of 4,6-diaminoresorcinol
US20050054586A1 (en) *	2003-06-30	2005-03-10	Bartels Stephen P.	Treatment of ophthalmic disorders

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DE141751C (de) *
FR499094A (fr) *	1919-04-17	1920-01-30	Joseph Cucumel	Machine pour le finissage des velours et tissus à poils
DE663552C (de) *	1935-09-29	1938-08-09	I G Farbenindustrie Akt Ges	Verfahren zur Herstellung von metallhaltigen Komplexverbindungen
GB663552A (en) *	1947-11-28	1951-12-27	Gen Aniline & Film Corp	Process of preparing 2,4-dihydroxybenzene-sulfonic acid
NL179175B (nl) *	1952-06-17		Rca Corp	In frequentie bestuurbare oscillator.
US3337549A (en) *	1962-11-08	1967-08-22	Keuffel & Esser Co	1-[tertiary amino-carbanilido]-3, 5-dihydroxy-4-bromo benzenes
DE1447733B2 (de) *	1963-12-23	1977-04-21	Hoechst Ag, 6000 Frankfurt	2-(3,5-dihydroxyphenyl)-benzimidazolderivate
DE1643400C3 (de) *	1966-11-22	1980-09-25	Basf Wyandotte Corp., Wyandotte, Mich. (V.St.A.)	Verwendung von 3-Benzoyl-4-hydroxy-6-methoxybenzolsulfonsäure als ultraviolett-Hchtabsorbierendes Mittel
FR1545111A (fr) *	1966-11-22	1968-11-08	Gen Aniline & Film Corp	Procédé perfectionné de préparation d'acide 3-benzoly-4-hydroxy-6-méthoxybenzènesulfonique et produit obtenu par ce procédé
US3919322A (en) *	1969-01-22	1975-11-11	Hoffmann La Roche	3-Substituted -5-alkyl-2-cyclohexen-1-ones
US3770547A (en) *	1971-05-14	1973-11-06	Sloane Mfg Co R & G	Color bond surveillance system
US3790636A (en) *	1971-09-16	1974-02-05	Hoffmann La Roche	Process for the preparation of alkyl substituted resorcinols
US3713256A (en) *	1971-10-28	1973-01-30	Besenbruch Hofmann	Adjustable grinding tool for brake cylinders and the like
JPS5644413B2 (de) *	1973-05-12	1981-10-19
CH605827A5 (en) *	1973-11-08	1978-10-13	Hoffmann La Roche	2,4-diamino-5-(3,5-dialkoxy-4-halo-benzyl)-pyrimidines
SE419444B (sv) *	1973-11-08	1981-08-03	Hoffmann La Roche	Forfarande for framstellning av nya 2,4-diamino-5-bensylpyrimidinderivat
DE2616479C2 (de) *	1976-04-14	1986-12-04	Brickl, Rolf, Dr., 7951 Warthausen	Substituierte Fluoracylresorcine, Verfahren zu ihrer Herstellung und diese enthaltende Arzneimittel und Kosmetika
IT1088554B (it) *	1977-11-17	1985-06-10	F I D I A Spa	Procedimento sellettivo per la preparazione di derivati della 7-indrossi cumarina
JPS555721A (en) *	1978-06-27	1980-01-16	Kawasaki Steel Corp	Detecting method for clogging of nozzle
EP0023673B1 (de) *	1979-08-03	1985-10-23	Kabushiki Kaisha Toshiba	Vorrichtung zum Aufzeichen mit Hilfe von Wärme, wärmeempfindliches Aufzeichnungsblatt und Verfahren zum Herstellen von Aufzeichnungen mit Hilfe von Wärme
JPS5644413A (en) *	1979-09-18	1981-04-23	Honda Motor Co Ltd	Device for introducing secondary air in engine
DD147424A1 (de) *	1979-11-28	1981-04-01	Detlef Rehorek	Ein-oder zweikomponentendiazotypiematerial
JPS56111849A (en) *	1980-02-12	1981-09-03	Konishiroku Photo Ind Co Ltd	Silver halide photographic sensitive material
DE3016905A1 (de) *	1980-05-02	1981-11-05	Henkel KGaA, 4000 Düsseldorf	Haarfaerbemittel
DE3044128A1 (de) *	1980-11-24	1982-07-15	Bayer Ag, 5090 Leverkusen	Cumarine, verfahren zu ihrer herstellung und ihre verwendung
JPS5934530A (ja) *	1982-08-23	1984-02-24	Konishiroku Photo Ind Co Ltd	ハロゲン化銀写真感光材料

1983
- 1983-12-21 IT IT8349556A patent/IT1212907B/it active
1984
- 1984-12-11 IL IL73787A patent/IL73787A/xx unknown
- 1984-12-11 IN IN863/CAL/84A patent/IN163437B/en unknown
- 1984-12-12 ES ES538544A patent/ES8604845A1/es not_active Expired
- 1984-12-12 ZA ZA849669A patent/ZA849669B/xx unknown
- 1984-12-14 MX MX203758A patent/MX162546A/es unknown
- 1984-12-18 NZ NZ210605A patent/NZ210605A/xx unknown
- 1984-12-18 FR FR8419343A patent/FR2557096B1/fr not_active Expired
- 1984-12-19 FI FI845035A patent/FI84907C/fi not_active IP Right Cessation
- 1984-12-19 EP EP84115842A patent/EP0146923B1/de not_active Expired - Lifetime
- 1984-12-19 CA CA000470581A patent/CA1325812C/en not_active Expired - Fee Related
- 1984-12-19 KR KR1019840008110A patent/KR880000202B1/ko not_active Expired
- 1984-12-19 AT AT84115842T patent/ATE65076T1/de active
- 1984-12-19 DE DE8484115842T patent/DE3484792D1/de not_active Expired - Lifetime
- 1984-12-20 PT PT79716A patent/PT79716A/pt not_active IP Right Cessation
- 1984-12-20 LU LU85703A patent/LU85703A1/fr unknown
- 1984-12-20 JP JP59270575A patent/JPH0635408B2/ja not_active Expired - Lifetime
- 1984-12-20 AU AU37117/84A patent/AU3711784A/en not_active Abandoned
- 1984-12-20 GR GR82532A patent/GR82532B/el unknown
- 1984-12-20 NO NO845150A patent/NO164235C/no unknown
- 1984-12-20 BR BR8406649A patent/BR8406649A/pt not_active IP Right Cessation
- 1984-12-20 CH CH6084/84A patent/CH666257A5/fr not_active IP Right Cessation
- 1984-12-20 IE IE3276/84A patent/IE57964B1/en not_active IP Right Cessation
- 1984-12-20 HU HU844755A patent/HU196938B/hu not_active IP Right Cessation
- 1984-12-20 BE BE1/11161A patent/BE901323A/fr not_active IP Right Cessation
- 1984-12-21 AR AR299067A patent/AR240908A1/es active
- 1984-12-21 DK DK625284A patent/DK625284A/da not_active Application Discontinuation
- 1984-12-21 US US06/684,733 patent/US4704469A/en not_active Expired - Lifetime
- 1984-12-21 YU YU2183/84A patent/YU44992B/xx unknown
1989
- 1989-07-06 AU AU37925/89A patent/AU618819B2/en not_active Ceased
1992
- 1992-11-18 JP JP4308634A patent/JPH0788349B2/ja not_active Ceased

Also Published As

Publication number	Publication date
DK625284D0 (da)	1984-12-21
ES538544A0 (es)	1986-02-16
JPH05345738A (ja)	1993-12-27
AU3792589A (en)	1989-10-19
AR240908A2 (es)	1991-03-27
PT79716A (en)	1985-01-01
KR880000202B1 (ko)	1988-03-12
YU44992B (en)	1991-06-30
FI84907B (fi)	1991-10-31
IL73787A0 (en)	1985-03-31
US4704469A (en)	1987-11-03
GR82532B (en)	1985-04-17
EP0146923A1 (de)	1985-07-03
CA1325812C (en)	1994-01-04
FI845035A0 (fi)	1984-12-19
ZA849669B (en)	1986-02-26
BR8406649A (pt)	1985-10-15
FI845035L (fi)	1985-06-22
NO164235C (no)	1990-09-12
MX162546A (es)	1991-05-20
IT1212907B (it)	1989-11-30
KR850004563A (ko)	1985-07-25
FI84907C (fi)	1992-02-10
NO164235B (no)	1990-06-05
ATE65076T1 (de)	1991-07-15
IE57964B1 (en)	1993-06-02
ES8604845A1 (es)	1986-02-16
HUT36443A (en)	1985-09-30
IL73787A (en)	1990-01-18
IE843276L (en)	1985-06-21
CH666257A5 (fr)	1988-07-15
IN163437B (de)	1988-09-24
NO845150L (no)	1985-06-24
HU196938B (en)	1989-02-28
NZ210605A (en)	1988-08-30
AU618819B2 (en)	1992-01-09
AR240908A1 (es)	1991-03-27
YU218384A (en)	1986-12-31
DK625284A (da)	1985-06-22
BE901323A (fr)	1985-06-20
JPH0635408B2 (ja)	1994-05-11
AU3711784A (en)	1985-07-04
FR2557096B1 (fr)	1988-09-30
JPH0788349B2 (ja)	1995-09-27
IT8349556A0 (it)	1983-12-21
JPS60156627A (ja)	1985-08-16
EP0146923B1 (de)	1991-07-10
FR2557096A1 (fr)	1985-06-28
DE3484792D1 (de)	1991-08-14

Publication	Publication Date	Title
EP0149407B1 (de)	1987-04-01	Verfahren zur Herstellung von Brombenzaldehyden-Hydroxy und/oder Alkoxy substituiert
FR2529886A1 (fr)	1984-01-13	Procede de preparation d'arylalcanoates a partir de 1-halogenalkylarylcetals catalyses par des carboxylates de zinc
EP0377381A1 (de)	1990-07-11	Verfahren zur Herstellung von 1-Phenyl-2-diethyl-aminocarbonyl-2-phthalimidomethyl-cyclopropan Z
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EP0149952B1 (de)	1987-07-08	Verfahren zur Herstellung von Brombenzaldehyden-Hydroxy und/oder Alkoxy substituiert
WO2004007424A1 (fr)	2004-01-22	Procede de preparation d'un nitrophenol
CH666257A5 (fr)	1988-07-15	Procede de preparation de 2-halogeno-resorcinols.
EP0200840B1 (de)	1989-04-05	Verfahren zur Herstellung von gegebenenfalls in 5-Stellung halogenisierten 6-(Nieder)-alkoxy-1-naphthoesäuren und den entsprechenden Estern
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CH623303A5 (de)	1981-05-29
EP0072293B1 (de)	1985-10-09	Verfahren zur Herstellung von Ursodeoxy-Cholsäure ausgehend von 3-alpha, 7-beta, 12-alpha-trihydroxy-Cholsäure und verwendete Zwischenprodukte
EP0278822B1 (de)	1990-05-23	Verfahren zur Herstellung von Perhalogenalkansulfin- und -sulfonsäureabkömmlingen
CH648329A5 (fr)	1985-03-15	Procede de preparation de steroides.
EP0195171B1 (de)	1989-03-29	Verfahren zur Herstellung von Monochlorhydrochinonen
FR2540860A1 (fr)	1984-08-17	Nouveaux intermediaires pour la production de derives de l'acide 2-(2-aminothiazol-4-yl) glyoxylique ou d'un de ses sels et le procede de production desdits intermediaires
FR2550190A1 (fr)	1985-02-08	Procede de preparation de b-phenylserine
WO2011098985A1 (fr)	2011-08-18	Procede de preparation de composes adamantyles
EP0767162B1 (de)	1999-12-08	Natrium-Orthohydroxymandelat-Phenol-Wasser-Komplexe, Verfahren zu deren Herstellung sowie Verwendung zur Isolation des Natrium Orthohydroxymandelats
EP0059659B1 (de)	1984-07-04	Derivate der 4-Methyl-3-formyl-pentansäure, ihr Herstellungsverfahren und Anwendung zur Herstellung von cyclischen Derivaten
FR2573754A1 (fr)	1986-05-30	Procede de preparation d'acides a-hydroxyphenylalcanoiques et composes obtenus par ce procede
CA1111447A (fr)	1981-10-27	Composes halogenes, procede de preparation et application a la preparation du metaphenoxy benzaldehyde
EP0860443A1 (de)	1998-08-26	Industrialisierungsverfahren zur Herstellung von Diosmin aus Hesperidin
EP0290319B1 (de)	1990-08-08	1-Fluor-1-halogen dioxa-3,6-bizyklo[4.1.0]heptan, Verfahren zur Herstellung und Verwendung
EP0495952A1 (de)	1992-07-29	Verfahren zur herstellung von 2-nitrobenzaldehyd- und nitrobenzoesäurederivate
FR2819807A1 (fr)	2002-07-26	Procede de synthese de l'acide dihydroxymalonique et de ses sels dibasiques