DD143609A5 - Verfahren zur herstellung von di-bzw.tri-isatosaeure-derivaten - Google Patents

Verfahren zur herstellung von di-bzw.tri-isatosaeure-derivaten Download PDF

Info

Publication number: DD143609A5
Authority: DD; German Democratic Republic
Prior art keywords: general formula; radical; formula; compound; isatoic anhydride
Prior art date: 1979-04-10

Application number

DD79212125A

Other languages

German (de)

English (en)

Inventor

Oskar Schmidt

Walter Sibral

Original Assignee

Lim Holding Sa

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.)

1979-04-10

Filing date

1979-04-10

Publication date

1980-09-03

1979-04-10 Application filed by Lim Holding Sa filed Critical Lim Holding Sa

1979-04-10 Priority to ZA791723A priority Critical patent/ZA791723B/xx

1979-04-10 Priority to BE0/194501A priority patent/BE875452A/fr

1979-04-10 Priority to AU45999/79A priority patent/AU4599979A/en

1979-04-10 Priority to SE7903189A priority patent/SE7903189L/xx

1979-04-10 Priority to FR7909078A priority patent/FR2453856A1/fr

1979-04-10 Priority to IT21741/79A priority patent/IT1111921B/it

1979-04-10 Priority to JP4356679A priority patent/JPS55139345A/ja

1979-04-10 Priority to GB7912634A priority patent/GB2046244A/en

1979-04-10 Priority to DD79212125A priority patent/DD143609A5/de

1979-04-10 Priority to BR7902207A priority patent/BR7902207A/pt

1979-04-10 Priority to NL7902829A priority patent/NL7902829A/nl

1979-04-10 Priority to US06/028,754 priority patent/US4283548A/en

1979-04-10 Priority to DE19792914545 priority patent/DE2914545A1/de

1980-09-03 Publication of DD143609A5 publication Critical patent/DD143609A5/de

Links

238000002360 preparation method Methods 0.000 title claims abstract description 25
238000000034 method Methods 0.000 title claims description 28
150000001875 compounds Chemical class 0.000 claims abstract description 54
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 16
229910052717 sulfur Inorganic materials 0.000 claims abstract description 14
229910052760 oxygen Inorganic materials 0.000 claims abstract description 11
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 10
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 10
239000001301 oxygen Substances 0.000 claims abstract description 10
239000011593 sulfur Substances 0.000 claims abstract description 10
125000002947 alkylene group Chemical group 0.000 claims abstract description 9
VYFOAVADNIHPTR-UHFFFAOYSA-N isatoic anhydride Chemical compound NC1=CC=CC=C1CO VYFOAVADNIHPTR-UHFFFAOYSA-N 0.000 claims description 33
229910052739 hydrogen Inorganic materials 0.000 claims description 10
125000001424 substituent group Chemical group 0.000 claims description 10
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 7
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 6
239000001257 hydrogen Substances 0.000 claims description 6
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 6
239000005977 Ethylene Substances 0.000 claims description 5
150000002009 diols Chemical class 0.000 claims description 4
229910052757 nitrogen Inorganic materials 0.000 claims description 4
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 4
GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 claims description 3
101150065749 Churc1 gene Proteins 0.000 claims description 3
102100038239 Protein Churchill Human genes 0.000 claims description 3
XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical compound ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 claims description 3
239000002253 acid Substances 0.000 claims description 3
125000000217 alkyl group Chemical group 0.000 claims description 3
229910052801 chlorine Inorganic materials 0.000 claims description 3
125000000623 heterocyclic group Chemical group 0.000 claims description 3
150000002431 hydrogen Chemical class 0.000 claims description 3
125000004430 oxygen atom Chemical group O* 0.000 claims description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
150000001555 benzenes Chemical class 0.000 claims description 2
125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
239000003960 organic solvent Substances 0.000 claims description 2
125000004434 sulfur atom Chemical group 0.000 claims description 2
239000004033 plastic Substances 0.000 abstract description 14
229920003023 plastic Polymers 0.000 abstract description 14
239000004970 Chain extender Substances 0.000 abstract description 7
238000006243 chemical reaction Methods 0.000 abstract description 7
239000004814 polyurethane Substances 0.000 abstract description 6
229920002635 polyurethane Polymers 0.000 abstract description 6
229920002396 Polyurea Polymers 0.000 abstract description 5
239000000376 reactant Substances 0.000 abstract description 2
125000001997 phenyl group Chemical class [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
239000005056 polyisocyanate Substances 0.000 description 43
229920001228 polyisocyanate Polymers 0.000 description 43
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 27
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 21
-1 alkyl radical Chemical class 0.000 description 15
150000003254 radicals Chemical group 0.000 description 14
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
239000012948 isocyanate Substances 0.000 description 12
150000002513 isocyanates Chemical class 0.000 description 11
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 10
239000013078 crystal Substances 0.000 description 10
OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical compound NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 description 8
239000000203 mixture Substances 0.000 description 8
XYKIUTSFQGXHOW-UHFFFAOYSA-N propan-2-one;toluene Chemical compound CC(C)=O.CC1=CC=CC=C1 XYKIUTSFQGXHOW-UHFFFAOYSA-N 0.000 description 7
JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 6
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
239000000460 chlorine Substances 0.000 description 6
IDGUHHHQCWSQLU-UHFFFAOYSA-N ethanol;hydrate Chemical compound O.CCO IDGUHHHQCWSQLU-UHFFFAOYSA-N 0.000 description 6
239000000741 silica gel Substances 0.000 description 6
229910002027 silica gel Inorganic materials 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical group OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 5
238000003756 stirring Methods 0.000 description 5
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 4
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 4
150000002148 esters Chemical class 0.000 description 4
239000000706 filtrate Substances 0.000 description 4
238000004519 manufacturing process Methods 0.000 description 4
239000002244 precipitate Substances 0.000 description 4
239000011541 reaction mixture Substances 0.000 description 4
238000010992 reflux Methods 0.000 description 4
229910052938 sodium sulfate Inorganic materials 0.000 description 4
235000011152 sodium sulphate Nutrition 0.000 description 4
239000007858 starting material Substances 0.000 description 4
FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 4
HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
239000003054 catalyst Substances 0.000 description 3
238000002425 crystallisation Methods 0.000 description 3
230000008025 crystallization Effects 0.000 description 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
239000003208 petroleum Substances 0.000 description 3
238000010626 work up procedure Methods 0.000 description 3
UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 2
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 2
239000000654 additive Substances 0.000 description 2
125000003277 amino group Chemical group 0.000 description 2
238000005266 casting Methods 0.000 description 2
238000009833 condensation Methods 0.000 description 2
230000005494 condensation Effects 0.000 description 2
150000004985 diamines Chemical class 0.000 description 2
239000003995 emulsifying agent Substances 0.000 description 2
WJRBRSLFGCUECM-UHFFFAOYSA-N hydantoin Chemical compound O=C1CNC(=O)N1 WJRBRSLFGCUECM-UHFFFAOYSA-N 0.000 description 2
229940091173 hydantoin Drugs 0.000 description 2
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 2
239000007788 liquid Substances 0.000 description 2
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
239000000047 product Substances 0.000 description 2
HYHCSLBZRBJJCH-UHFFFAOYSA-M sodium hydrosulfide Chemical compound [Na+].[SH-] HYHCSLBZRBJJCH-UHFFFAOYSA-M 0.000 description 2
238000004809 thin layer chromatography Methods 0.000 description 2
ATIAIEWDRRJGSL-UHFFFAOYSA-N 1,3-bis(2-hydroxyethyl)-5,5-dimethylimidazolidine-2,4-dione Chemical compound CC1(C)N(CCO)C(=O)N(CCO)C1=O ATIAIEWDRRJGSL-UHFFFAOYSA-N 0.000 description 1
OVBFMUAFNIIQAL-UHFFFAOYSA-N 1,4-diisocyanatobutane Chemical compound O=C=NCCCCN=C=O OVBFMUAFNIIQAL-UHFFFAOYSA-N 0.000 description 1
FRASJONUBLZVQX-UHFFFAOYSA-N 1,4-naphthoquinone Chemical compound C1=CC=C2C(=O)C=CC(=O)C2=C1 FRASJONUBLZVQX-UHFFFAOYSA-N 0.000 description 1
WEGOLYBUWCMMMY-UHFFFAOYSA-N 1-bromo-2-propanol Chemical compound CC(O)CBr WEGOLYBUWCMMMY-UHFFFAOYSA-N 0.000 description 1
RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
WTPYFJNYAMXZJG-UHFFFAOYSA-N 2-[4-(2-hydroxyethoxy)phenoxy]ethanol Chemical compound OCCOC1=CC=C(OCCO)C=C1 WTPYFJNYAMXZJG-UHFFFAOYSA-N 0.000 description 1
HMAAFPUFWDBSRM-UHFFFAOYSA-N 2-[4-(2-sulfanylethoxy)phenoxy]ethanethiol Chemical compound SCCOC1=CC=C(OCCS)C=C1 HMAAFPUFWDBSRM-UHFFFAOYSA-N 0.000 description 1
QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 1
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 1
239000005058 Isophorone diisocyanate Substances 0.000 description 1
238000005684 Liebig rearrangement reaction Methods 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
125000003368 amide group Chemical group 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
150000001448 anilines Chemical class 0.000 description 1
150000004984 aromatic diamines Chemical class 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
230000000711 cancerogenic effect Effects 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
238000004587 chromatography analysis Methods 0.000 description 1
229940125890 compound Ia Drugs 0.000 description 1
238000001816 cooling Methods 0.000 description 1
150000001913 cyanates Chemical class 0.000 description 1
125000005442 diisocyanate group Chemical group 0.000 description 1
OPTDDWCXQQYKGU-UHFFFAOYSA-N diphenyldichloromethane Chemical compound C=1C=CC=CC=1C(Cl)(Cl)C1=CC=CC=C1 OPTDDWCXQQYKGU-UHFFFAOYSA-N 0.000 description 1
238000004049 embossing Methods 0.000 description 1
NLFBCYMMUAKCPC-KQQUZDAGSA-N ethyl (e)-3-[3-amino-2-cyano-1-[(e)-3-ethoxy-3-oxoprop-1-enyl]sulfanyl-3-oxoprop-1-enyl]sulfanylprop-2-enoate Chemical compound CCOC(=O)\C=C\SC(=C(C#N)C(N)=O)S\C=C\C(=O)OCC NLFBCYMMUAKCPC-KQQUZDAGSA-N 0.000 description 1
OAMZXMDZZWGPMH-UHFFFAOYSA-N ethyl acetate;toluene Chemical compound CCOC(C)=O.CC1=CC=CC=C1 OAMZXMDZZWGPMH-UHFFFAOYSA-N 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000012467 final product Substances 0.000 description 1
239000003063 flame retardant Substances 0.000 description 1
DYDNPESBYVVLBO-UHFFFAOYSA-N formanilide Chemical compound O=CNC1=CC=CC=C1 DYDNPESBYVVLBO-UHFFFAOYSA-N 0.000 description 1
235000019253 formic acid Nutrition 0.000 description 1
239000007789 gas Substances 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
239000011874 heated mixture Substances 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
239000007791 liquid phase Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
229960005323 phenoxyethanol Drugs 0.000 description 1
125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
239000001294 propane Substances 0.000 description 1
239000002994 raw material Substances 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000010409 thin film Substances 0.000 description 1
DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 description 1
150000004072 triols Chemical class 0.000 description 1
AVWRKZWQTYIKIY-UHFFFAOYSA-N urea-1-carboxylic acid Chemical compound NC(=O)NC(O)=O AVWRKZWQTYIKIY-UHFFFAOYSA-N 0.000 description 1
150000003673 urethanes Chemical class 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
- C08G18/3819—Low-molecular-weight compounds having heteroatoms other than oxygen having nitrogen
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C327/00—Thiocarboxylic acids
- C07C327/20—Esters of monothiocarboxylic acids
- C07C327/28—Esters of monothiocarboxylic acids having sulfur atoms of esterified thiocarboxyl groups bound to carbon atoms of hydrocarbon radicals substituted by singly-bound oxygen atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/20—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
- C07C43/225—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing halogen
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/20—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
- C07C43/23—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing hydroxy or O-metal groups
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/72—Two oxygen atoms, e.g. hydantoin
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/72—Two oxygen atoms, e.g. hydantoin
- C07D233/74—Two oxygen atoms, e.g. hydantoin with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to other ring members
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/72—Two oxygen atoms, e.g. hydantoin
- C07D233/76—Two oxygen atoms, e.g. hydantoin with substituted hydrocarbon radicals attached to the third ring carbon atom
- C07D233/78—Radicals substituted by oxygen atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
- C07D235/26—Oxygen atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/68—Benzothiazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
- C07D277/70—Sulfur atoms
- C07D277/76—Sulfur atoms attached to a second hetero atom
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
- C08G18/3225—Polyamines
- C08G18/3237—Polyamines aromatic
- C08G18/3243—Polyamines aromatic containing two or more aromatic rings
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Indole Compounds (AREA)
Polyurethanes Or Polyureas (AREA)

DD79212125A 1979-04-10 1979-04-10 Verfahren zur herstellung von di-bzw.tri-isatosaeure-derivaten DD143609A5 (de)

Priority Applications (13)

Application Number	Priority Date	Filing Date	Title
ZA791723A ZA791723B (en)	1979-04-10	1979-04-10	Disatoic acid or triisatoic acid derivatives processes for their production and their use
BE0/194501A BE875452A (fr)	1979-04-10	1979-04-10	Nouveaux derives d'acides di- ou tri-isatiniques, procedes de realisation et modes d'application
AU45999/79A AU4599979A (en)	1979-04-10	1979-04-10	Diisatoic acid or triisatoic acid derivatives
SE7903189A SE7903189L (sv)	1979-04-10	1979-04-10	Di- eller triisatosyraderivat, forfarande for dess framstellning samt anvendning derav
FR7909078A FR2453856A1 (fr)	1979-04-10	1979-04-10	Nouveaux derives d'acides di- ou triisatiniques, procedes de realisation, et modes d'application
IT21741/79A IT1111921B (it)	1979-04-10	1979-04-10	Di-e/o tri-derivati dell'acido o-carbossifenilcarbammico,procedimento per la loro produzione e loro impiego
JP4356679A JPS55139345A (en)	1979-04-10	1979-04-10	Derivative of diisatoic acid or triisatoic acid and its manufacture and use
GB7912634A GB2046244A (en)	1979-04-10	1979-04-10	Novel diisatoic and triisatoic acid derivatives
DD79212125A DD143609A5 (de)	1979-04-10	1979-04-10	Verfahren zur herstellung von di-bzw.tri-isatosaeure-derivaten
BR7902207A BR7902207A (pt)	1979-04-10	1979-04-10	Compostos organicos,processo para sua preparacao e seu emprego
NL7902829A NL7902829A (nl)	1979-04-10	1979-04-10	Di- en tri-isotazuurderivaten, hun bereiding en toepassing.
US06/028,754 US4283548A (en)	1979-04-10	1979-04-10	Diisatoic acid or triisatoic acid derivatives
DE19792914545 DE2914545A1 (de)	1979-04-10	1979-04-10	Di- bzw. tri-isatosaeure-derivate, verfahren zu deren herstellung und deren verwendung

Applications Claiming Priority (13)

Application Number	Priority Date	Filing Date	Title
ZA791723A ZA791723B (en)	1979-04-10	1979-04-10	Disatoic acid or triisatoic acid derivatives processes for their production and their use
BE0/194501A BE875452A (fr)	1979-04-10	1979-04-10	Nouveaux derives d'acides di- ou tri-isatiniques, procedes de realisation et modes d'application
AU45999/79A AU4599979A (en)	1979-04-10	1979-04-10	Diisatoic acid or triisatoic acid derivatives
SE7903189A SE7903189L (sv)	1979-04-10	1979-04-10	Di- eller triisatosyraderivat, forfarande for dess framstellning samt anvendning derav
FR7909078A FR2453856A1 (fr)	1979-04-10	1979-04-10	Nouveaux derives d'acides di- ou triisatiniques, procedes de realisation, et modes d'application
IT21741/79A IT1111921B (it)	1979-04-10	1979-04-10	Di-e/o tri-derivati dell'acido o-carbossifenilcarbammico,procedimento per la loro produzione e loro impiego
JP4356679A JPS55139345A (en)	1979-04-10	1979-04-10	Derivative of diisatoic acid or triisatoic acid and its manufacture and use
GB7912634A GB2046244A (en)	1979-04-10	1979-04-10	Novel diisatoic and triisatoic acid derivatives
DD79212125A DD143609A5 (de)	1979-04-10	1979-04-10	Verfahren zur herstellung von di-bzw.tri-isatosaeure-derivaten
BR7902207A BR7902207A (pt)	1979-04-10	1979-04-10	Compostos organicos,processo para sua preparacao e seu emprego
NL7902829A NL7902829A (nl)	1979-04-10	1979-04-10	Di- en tri-isotazuurderivaten, hun bereiding en toepassing.
US06/028,754 US4283548A (en)	1979-04-10	1979-04-10	Diisatoic acid or triisatoic acid derivatives
DE19792914545 DE2914545A1 (de)	1979-04-10	1979-04-10	Di- bzw. tri-isatosaeure-derivate, verfahren zu deren herstellung und deren verwendung

Publications (1)

Publication Number	Publication Date
DD143609A5 true DD143609A5 (de)	1980-09-03

Family

ID=27583886

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD79212125A DD143609A5 (de)	1979-04-10	1979-04-10	Verfahren zur herstellung von di-bzw.tri-isatosaeure-derivaten

Country Status (13)

Country	Link
US (1)	US4283548A (fr)
JP (1)	JPS55139345A (fr)
AU (1)	AU4599979A (fr)
BE (1)	BE875452A (fr)
BR (1)	BR7902207A (fr)
DD (1)	DD143609A5 (fr)
DE (1)	DE2914545A1 (fr)
FR (1)	FR2453856A1 (fr)
GB (1)	GB2046244A (fr)
IT (1)	IT1111921B (fr)
NL (1)	NL7902829A (fr)
SE (1)	SE7903189L (fr)
ZA (1)	ZA791723B (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
KR102505374B1 (ko) *	2016-10-06	2023-03-02	닛산 가가쿠 가부시키가이샤	디아민, 중합체, 액정 배향제, 액정 배향막 및 액정 표시 소자
KR102980361B1 (ko)	2019-01-28	2026-06-23	닛산 가가쿠 가부시키가이샤	슬릿 다이 코트용 박리층 형성용 조성물 및 박리층
CN115537171A (zh) *	2022-09-27	2022-12-30	江苏华大新材料有限公司	一种耐低温聚氨酯复合胶及其制备方法

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4161594A (en) *	1968-11-11	1979-07-17	Ciba-Geigy Ag	Dialcohols
CH523279A (de) *	1968-11-11	1972-05-31	Ciba Geigy Ag	Verfahren zur Herstellung von neuen Diglycidylverbindungen von N-heterocyclischen Verbindungen und deren Verwendung
FR2148868A6 (fr) *	1970-10-06	1973-03-23	Rhone Poulenc Sa
CH546798A (de) *	1971-08-17	1974-03-15	Ciba Geigy Ag	Verfahren zum haerten von acrylsaeureesterderivaten mit ionisierenden strahlen.
CH570379A5 (fr) *	1972-07-12	1975-12-15	Ciba Geigy Ag
DD127235A5 (fr) *	1975-10-27	1977-09-14
US4129741A (en) *	1975-10-27	1978-12-12	Lim-Holding, S.A.	Novel polyethers having terminal amino groups, a process for their production and their application
US4122276A (en) *	1976-05-12	1978-10-24	Ciba-Geigy Corporation	Dicarboxylic acids and dicarboxylic acid esters containing a heterocyclic radical

1979
- 1979-04-10 ZA ZA791723A patent/ZA791723B/xx unknown
- 1979-04-10 US US06/028,754 patent/US4283548A/en not_active Expired - Lifetime
- 1979-04-10 AU AU45999/79A patent/AU4599979A/en not_active Abandoned
- 1979-04-10 SE SE7903189A patent/SE7903189L/xx not_active Application Discontinuation
- 1979-04-10 FR FR7909078A patent/FR2453856A1/fr not_active Withdrawn
- 1979-04-10 GB GB7912634A patent/GB2046244A/en not_active Withdrawn
- 1979-04-10 DE DE19792914545 patent/DE2914545A1/de not_active Ceased
- 1979-04-10 BR BR7902207A patent/BR7902207A/pt unknown
- 1979-04-10 DD DD79212125A patent/DD143609A5/de unknown
- 1979-04-10 JP JP4356679A patent/JPS55139345A/ja active Pending
- 1979-04-10 BE BE0/194501A patent/BE875452A/fr unknown
- 1979-04-10 IT IT21741/79A patent/IT1111921B/it active
- 1979-04-10 NL NL7902829A patent/NL7902829A/nl not_active Application Discontinuation

Also Published As

Publication number	Publication date
FR2453856A1 (fr)	1980-11-07
GB2046244A (en)	1980-11-12
DE2914545A1 (de)	1980-10-16
ZA791723B (en)	1980-04-30
JPS55139345A (en)	1980-10-31
IT7921741A0 (it)	1979-04-10
BR7902207A (pt)	1980-10-21
NL7902829A (nl)	1980-10-14
BE875452A (fr)	1979-10-10
US4283548A (en)	1981-08-11
AU4599979A (en)	1980-10-16
IT1111921B (it)	1986-01-13
SE7903189L (sv)	1980-10-11

Publication	Publication Date	Title
EP0417603B1 (fr)	2001-01-17	Procédé de préparation de polyisocyanates contenant des groupes urétidinedione
DE1174759B (de)	1964-07-30	Verfahren zur Herstellung von Polyisocyanaten mit Biuretstruktur
DE2316028A1 (de)	1973-11-22	Verfahren zur verringerung des gehalts an verbindungen mit hydrolysierbarem chlor und an sauer wirkenden verbindungen eines organischen isocyanats
EP0024665A1 (fr)	1981-03-11	Diisocyanates ou mélanges de diisocyanates de la série diphénylméthane, procédé pour leur préparation et leur utilisation comme produits de départ pour la préparation de polyuréthanes selon le procédé de polymérisation par addition d'isocyanates
EP0062823B1 (fr)	1985-01-30	Procédé de production de polyisocyanates aromatiques porteurs de groupes urée et/ou de groupes biuret et leur utilisation comme composant isocyanate dans la fabrication de polyuréthannes
EP0028829A1 (fr)	1981-05-20	Urées contenant des substituants cycliques, procédé pour les préparer et leur utilisation comme herbicides
DE3141815C2 (fr)	1988-06-30
DE1668170C (fr)	1973-08-23
EP0298336A1 (fr)	1989-01-11	Polyisocyanates aromatiques, un procédé pour leur préparation ainsi que leur utilisation comme composants d'adhésifs
DE3151855A1 (de)	1983-07-07	Neue isocyanato-isocyanurate sowie ein verfahren zu deren herstellung
DE2852785A1 (de)	1979-06-13	Anthranilsaeureester von oxyalkylierten carbonsaeureamiden
EP0000893A1 (fr)	1979-03-07	Procédé pour la préparation de polyisocyanates et leur utilisation
EP0148462B1 (fr)	1987-07-08	Procédé pour la préparation in situ de diisocyanates contenant des groupes urée dans des polyols, des dispersions ou des solutions selon ce procédé et leur utilisation
EP0071839B1 (fr)	1985-09-25	Diisocyanates aromatiques contenant des groupes sulphonamido N,N-disubstitués, leur méthode de préparation et leur emploi pour la préparation de polyuréthanes
DE2914545A1 (de)	1980-10-16	Di- bzw. tri-isatosaeure-derivate, verfahren zu deren herstellung und deren verwendung
EP0683154B1 (fr)	1998-08-19	Diisocyanates, procédé pour leur préparation et leur utilisation
DE1668170B2 (de)	1973-01-25	N-octahydro-1,2,4-methenopentalenyl(5)-harnstoffe, verfahren zu deren herstellung und deren verwendung als herbizide
EP0085880B1 (fr)	1985-09-11	Procédé pour la préparation de l'amide ester de l'acide éthène-1,2-dicarboxylique
EP0128382A1 (fr)	1984-12-19	Cyclohexanes 1-alcoyl-2-isocyanatométhylisocyanato et/ou 1-alcoyl-4-isocyanatométhylisocyanato et les diamines correspondantes, procédé pour leur fabric tion et utilisation
EP0040760B1 (fr)	1983-04-13	Procédé de fabrication d'isocyanates masqués
AT356085B (de)	1980-04-10	Verfahren zur herstellung von neuen anthranil- saeureestern
EP0191386B1 (fr)	1989-10-18	Dérivés polyhydroxylés contenant des groupements urée et ester ou amide, procédé de préparation et utilisation
DE2555830A1 (de)	1976-06-24	Verfahren zur herstellung von organischen isocyanaten
DE2945867A1 (de)	1981-06-04	Substituierte polyisocyanate oder polyisocyanatgemische der diphenylmethanreihe, die chlorsulfonylgruppen enthalten, ein verfahren zu ihrer herstellung, sowie ihre verwendung bei der herstellung von polyisocyanat-polyadditions-verbindungen
DE2206167B2 (de)	1973-12-13	Herstellung von herbicid wirk samen 3 (Halogenphenyl) 1,1 dialkyl harnstoffen