SU577998A3 - Способ получени ароматических бис-(эфиров ангидридов) - Google Patents
Способ получени ароматических бис-(эфиров ангидридов)Info
- Publication number
- SU577998A3 SU577998A3 SU7402018016A SU2018016A SU577998A3 SU 577998 A3 SU577998 A3 SU 577998A3 SU 7402018016 A SU7402018016 A SU 7402018016A SU 2018016 A SU2018016 A SU 2018016A SU 577998 A3 SU577998 A3 SU 577998A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- bis
- preparing aromatic
- mixture
- aromatic bis
- anhydride esters
- Prior art date
Links
- 238000000034 method Methods 0.000 title description 3
- 125000003118 aryl group Chemical group 0.000 title description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- ODLMAHJVESYWTB-UHFFFAOYSA-N propylbenzene Chemical compound CCCC1=CC=CC=C1 ODLMAHJVESYWTB-UHFFFAOYSA-N 0.000 description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 238000010992 reflux Methods 0.000 description 4
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 3
- -1 anhydride esters Chemical class 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 3
- 238000000921 elemental analysis Methods 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000012043 crude product Substances 0.000 description 2
- 229960001760 dimethyl sulfoxide Drugs 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- YKPAABNCNAGAAJ-UHFFFAOYSA-N 1,1-Bis(4-hydroxyphenyl)propane Chemical compound C=1C=C(O)C=CC=1C(CC)C1=CC=C(O)C=C1 YKPAABNCNAGAAJ-UHFFFAOYSA-N 0.000 description 1
- ZXDDPOHVAMWLBH-UHFFFAOYSA-N 2,4-Dihydroxybenzophenone Chemical compound OC1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 ZXDDPOHVAMWLBH-UHFFFAOYSA-N 0.000 description 1
- RXNYJUSEXLAVNQ-UHFFFAOYSA-N 4,4'-Dihydroxybenzophenone Chemical compound C1=CC(O)=CC=C1C(=O)C1=CC=C(O)C=C1 RXNYJUSEXLAVNQ-UHFFFAOYSA-N 0.000 description 1
- 125000004203 4-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- BGEBZHIAGXMEMV-UHFFFAOYSA-N 5-methoxypsoralen Chemical compound O1C(=O)C=CC2=C1C=C1OC=CC1=C2OC BGEBZHIAGXMEMV-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- GTDPSWPPOUPBNX-UHFFFAOYSA-N ac1mqpva Chemical compound CC12C(=O)OC(=O)C1(C)C1(C)C2(C)C(=O)OC1=O GTDPSWPPOUPBNX-UHFFFAOYSA-N 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 239000000010 aprotic solvent Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229940106691 bisphenol a Drugs 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 1
- 229960001755 resorcinol Drugs 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
- C07D209/48—Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Indole Compounds (AREA)
- Furan Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US346473A US3879428A (en) | 1973-03-30 | 1973-03-30 | Method for making aromatic bis(ether anhydride)s |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU577998A3 true SU577998A3 (ru) | 1977-10-25 |
Family
ID=23359545
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU7402018016A SU577998A3 (ru) | 1973-03-30 | 1974-03-29 | Способ получени ароматических бис-(эфиров ангидридов) |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US3879428A (cg-RX-API-DMAC7.html) |
| JP (1) | JPS596871B2 (cg-RX-API-DMAC7.html) |
| BR (1) | BR7402533D0 (cg-RX-API-DMAC7.html) |
| DD (1) | DD112980A5 (cg-RX-API-DMAC7.html) |
| DE (1) | DE2412466C2 (cg-RX-API-DMAC7.html) |
| FR (1) | FR2228050B1 (cg-RX-API-DMAC7.html) |
| GB (1) | GB1469482A (cg-RX-API-DMAC7.html) |
| IT (1) | IT1003928B (cg-RX-API-DMAC7.html) |
| SE (1) | SE419641B (cg-RX-API-DMAC7.html) |
| SU (1) | SU577998A3 (cg-RX-API-DMAC7.html) |
Families Citing this family (63)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3944583A (en) * | 1975-02-27 | 1976-03-16 | General Electric Company | Bis-phenoxyphthalic acid anhydrides |
| US3956322A (en) * | 1975-03-14 | 1976-05-11 | General Electric Company | Dianhydrides of bis-(orthodicarboxyphenyloxyphenyl)acetylene and bis-(ortho-dicarboxyphenyloxyphenyl)2,2-dichloroethylene |
| US4054600A (en) * | 1975-06-27 | 1977-10-18 | General Electric Company | Method for making aromatic bis(ether dicarboxylic acid)s |
| US4020069A (en) * | 1975-07-25 | 1977-04-26 | General Electric Company | Preparation of aromatic tetracarboxylic acids |
| US4005134A (en) * | 1975-09-11 | 1977-01-25 | General Electric Company | Method for making aromatic bis(ether dicarboxylic acid) |
| US4048190A (en) * | 1976-02-17 | 1977-09-13 | General Electric Company | Preparation of bisphenol-A bisimides |
| US4017511A (en) * | 1976-03-24 | 1977-04-12 | General Electric Company | Preparation of aromatic bisimides |
| US3992407A (en) * | 1976-04-14 | 1976-11-16 | General Electric Company | Preparation of aromatic bisimides |
| US4054577A (en) * | 1976-05-06 | 1977-10-18 | General Electric Company | Preparation of aromatic bisimides |
| US4196277A (en) * | 1976-07-19 | 1980-04-01 | Trw Inc. | Perfluoroisopropylidene dianhydride and polyimides prepared therefrom |
| US4217281A (en) * | 1976-10-04 | 1980-08-12 | General Electric Company | Imide carbonyl compounds and method for making |
| US4116980A (en) * | 1976-10-04 | 1978-09-26 | General Electric Company | Method for making aromatic bis (ether phthalic acid) or aromatic bis (ether anhydride)s |
| US4273712A (en) * | 1979-05-09 | 1981-06-16 | General Electric Company | Method for making aromatic ether imides |
| GB2096141B (en) * | 1981-04-03 | 1985-04-24 | Gen Electric | Method for making aromatic bis(ether phthalic acid) or aromatic bis(ether anhydride) |
| US4329292A (en) * | 1981-04-16 | 1982-05-11 | General Electric Company | Continuous method for making aromatic bis(ether phthalic acid) or aromatic bis(ether anhydride) |
| US4340545A (en) * | 1981-04-13 | 1982-07-20 | General Electric Company | Method for making aromatic bis(ether anhydrides) |
| US5512676A (en) * | 1987-09-03 | 1996-04-30 | The Boeing Company | Extended amideimide hub for multidimensional oligomers |
| US5693741A (en) * | 1988-03-15 | 1997-12-02 | The Boeing Company | Liquid molding compounds |
| US5969079A (en) * | 1985-09-05 | 1999-10-19 | The Boeing Company | Oligomers with multiple chemically functional end caps |
| US5506060A (en) * | 1981-11-13 | 1996-04-09 | The Boeing Company | Method for making multidimensional ether or ester oligomers |
| US5210213A (en) * | 1983-06-17 | 1993-05-11 | The Boeing Company | Dimensional, crosslinkable oligomers |
| US5516876A (en) * | 1983-09-27 | 1996-05-14 | The Boeing Company | Polyimide oligomers and blends |
| US5705598A (en) | 1985-04-23 | 1998-01-06 | The Boeing Company | Polyester sulfone oligomers and blends |
| US4476309A (en) * | 1983-03-21 | 1984-10-09 | General Electric Company | Method for making aromatic etherimides |
| US4623732A (en) * | 1983-11-18 | 1986-11-18 | General Electric Company | Process for the preparation of N-alkylphthalimide and copolymer derived therefrom |
| EP0184595A1 (en) * | 1984-12-14 | 1986-06-18 | General Electric Company | Process for the synthesis of N-alkylphthalimide |
| US4571425A (en) * | 1985-02-14 | 1986-02-18 | General Electric Company | Method for making aromatic bis(ether anhydride) |
| US5618907A (en) * | 1985-04-23 | 1997-04-08 | The Boeing Company | Thallium catalyzed multidimensional ester oligomers |
| US5610317A (en) * | 1985-09-05 | 1997-03-11 | The Boeing Company | Multiple chemically functional end cap monomers |
| JPH0655710B2 (ja) * | 1985-12-16 | 1994-07-27 | 東燃株式会社 | スルホニル基を有する芳香族化合物及びその製造法 |
| US4757149A (en) * | 1986-12-31 | 1988-07-12 | General Electric Company | Synthesis of bis(N-substituted phthalimide)ethers |
| US5068353A (en) * | 1986-12-31 | 1991-11-26 | General Electric Company | Synthesis of aromatic bis(ether phthalimide) compounds |
| US4864034A (en) * | 1988-01-20 | 1989-09-05 | General Electric Company | Spiro(bis)indane bis-oxyphthalic acids and functional derivatives thereof |
| US5817744A (en) * | 1988-03-14 | 1998-10-06 | The Boeing Company | Phenylethynyl capped imides |
| US5101006A (en) * | 1989-05-15 | 1992-03-31 | Occidental Chemical Corporation | Polyimides and copolyimides based on halo-oxydiphthalic anhydrides |
| US5185451A (en) * | 1989-05-15 | 1993-02-09 | Occidental Chemical Corporation | Bis-imides of dioxydiphthalic acid |
| US5166404A (en) * | 1989-05-15 | 1992-11-24 | Occidental Chemical Corporation | Dioxydiphthalic acid esters |
| US5262516A (en) * | 1991-11-26 | 1993-11-16 | General Electric Company | Method for preparing polyetherimide-polyamide copolymers |
| US5359084A (en) * | 1993-02-18 | 1994-10-25 | General Electric Company | Method of preparing aromatic ether bisimides |
| US5434240A (en) * | 1994-04-29 | 1995-07-18 | The University Of Liverpool | Poly (imide-ethers) |
| US6008374A (en) * | 1994-05-27 | 1999-12-28 | General Electric Company | Process for preparing bis (ether anhydrides) using alkylamine derived bisimides having low melting temperatures |
| TW399043B (en) * | 1994-05-27 | 2000-07-21 | Gen Electric | Process for preparing bis (ether anhydrides) using alkylamine derived bisimides having low melting temperatures |
| US5536846A (en) * | 1994-05-27 | 1996-07-16 | General Electric Company | Process for preparing bis(ether anhydrides) using alkylamine derived bisimides having low melting temperatures |
| US6576770B1 (en) | 2001-12-05 | 2003-06-10 | General Electric Company | Preparation of substituted phthalic anhydrides and substituted phthalimides |
| US6498224B1 (en) * | 2001-12-05 | 2002-12-24 | General Electric Company | Methods for the preparation poly(etherimide)s |
| US6528663B1 (en) | 2001-12-05 | 2003-03-04 | General Electric Company | Methods for the preparation of 4-chlorophthalic anhydride |
| US6881815B2 (en) * | 2002-09-25 | 2005-04-19 | General Electric Company | Method for the preparation poly(etherimide)s |
| US7115785B2 (en) * | 2003-08-25 | 2006-10-03 | General Electric Company | Method for making salts hydroxy-substituted hydrocarbons |
| EP1776094A2 (en) * | 2004-08-06 | 2007-04-25 | Grain Processing Corporation | Tablet coating composition |
| US7902407B2 (en) | 2005-03-30 | 2011-03-08 | Sabic Innovative Plastics Ip B.V. | Method for preparation of salts of hydroxy-substituted aromatic compounds |
| US8080671B2 (en) | 2008-05-23 | 2011-12-20 | Sabic Innovative Plastics Ip B.V. | Production of low color polyetherimides |
| WO2017117449A1 (en) * | 2015-12-29 | 2017-07-06 | Sabic Global Technologies B.V. | Methods for the manufacture of an aromatic bisimide and a polyetherimide |
| EP3397672A1 (en) | 2015-12-31 | 2018-11-07 | SABIC Global Technologies B.V. | Polyetherimide compositions, methods of manufacture, and articles prepared therefrom |
| WO2017172593A1 (en) * | 2016-03-29 | 2017-10-05 | Sabic Global Technologies B.V. | Methods of manufacture of bis(ether anhydride)s and polyetherimides |
| CN106279085B (zh) * | 2016-08-17 | 2018-07-10 | 万华化学集团股份有限公司 | 一种混合异构双醚四甲酸二酐的制备方法 |
| CN107987007B (zh) * | 2017-11-21 | 2020-07-24 | 万华化学集团股份有限公司 | N-烃基-n’-烃基双醚型双邻苯二甲酰亚胺的制备方法 |
| US12258448B2 (en) | 2019-01-31 | 2025-03-25 | Shpp Global Technologies B.V. | Method of making a biphenol dianhydride composition, method for purification of a biphenol dianhydride composition, and poly (etherimides) derived from the biphenol dianhydride |
| CN113330003B (zh) | 2019-01-31 | 2025-07-01 | 高新特殊工程塑料全球技术有限公司 | 制备联苯酚二酐组合物的方法、纯化联苯酚二酐的方法以及衍生自联苯酚二酐的聚(醚酰亚胺) |
| EP3917917A1 (en) | 2019-01-31 | 2021-12-08 | SHPP Global Technologies B.V. | Method for purification of a bisphenol a dianhydride composition, bisphenol a dianhydride composition, poly(etherimide) derived from the bisphenol a dianhydride composition, and articles prepared therefrom |
| EP3917905A1 (en) | 2019-01-31 | 2021-12-08 | SHPP Global Technologies B.V. | Method for purification of a biphenol tetraacid composition and a biphenol tetraacid composition |
| WO2021113491A1 (en) | 2019-12-03 | 2021-06-10 | Shpp Global Technologies B.V. | Polyimide varnish from high purity bisphenol a dianhydride and articles prepared therefrom |
| WO2021113489A1 (en) | 2019-12-03 | 2021-06-10 | Shpp Global Technologies B.V. | Polyamic acid varnish from high purity bisphenol a dianhydride and articles prepared therefrom |
| CN119487001A (zh) | 2022-07-01 | 2025-02-18 | 高新特殊工程塑料全球技术有限公司 | 3,3’-芳香族双(醚酰亚胺)、其聚醚酰亚胺及其制备方法 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3787475A (en) * | 1971-01-20 | 1974-01-22 | Gen Electric | Process for making aryloxy derivatives of aromatic diesters and dinitriles |
| US3965125A (en) * | 1971-02-08 | 1976-06-22 | Trw Inc. | Synthesis of certain bis(phthalic anhydrides) |
| US3734926A (en) * | 1971-10-04 | 1973-05-22 | Ciba Geigy Corp | Benzophenone-3,4,3{40 ,4-tetracarboxylic acid diimides of 3,5-dialkyl-4-hydroxyphenylsubstituted amines |
| US3746721A (en) * | 1971-10-04 | 1973-07-17 | Ciba Geigy Corp | Aromatic diimides of 3,5-dialkyl-4-hydroxyphenylsubstituted amines |
| DE2261715A1 (de) * | 1972-12-16 | 1974-06-20 | Gen Electric | Polyaetherimide und verfahren zu deren herstellung |
| DE2261714A1 (de) * | 1972-12-16 | 1974-06-20 | Gen Electric | Bis(nitrophthalimide) |
-
1973
- 1973-03-30 US US346473A patent/US3879428A/en not_active Expired - Lifetime
-
1974
- 1974-03-15 DE DE2412466A patent/DE2412466C2/de not_active Expired
- 1974-03-22 GB GB1286774A patent/GB1469482A/en not_active Expired
- 1974-03-26 FR FR7410289A patent/FR2228050B1/fr not_active Expired
- 1974-03-27 IT IT49728/74A patent/IT1003928B/it active
- 1974-03-28 DD DD177527A patent/DD112980A5/xx unknown
- 1974-03-29 BR BR2533/74A patent/BR7402533D0/pt unknown
- 1974-03-29 SE SE7404314A patent/SE419641B/xx not_active IP Right Cessation
- 1974-03-29 SU SU7402018016A patent/SU577998A3/ru active
- 1974-03-29 JP JP49034777A patent/JPS596871B2/ja not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| DD112980A5 (cg-RX-API-DMAC7.html) | 1975-05-12 |
| GB1469482A (en) | 1977-04-06 |
| JPS596871B2 (ja) | 1984-02-15 |
| DE2412466A1 (de) | 1974-10-10 |
| FR2228050A1 (cg-RX-API-DMAC7.html) | 1974-11-29 |
| JPS5024242A (cg-RX-API-DMAC7.html) | 1975-03-15 |
| US3879428A (en) | 1975-04-22 |
| FR2228050B1 (cg-RX-API-DMAC7.html) | 1979-04-20 |
| DE2412466C2 (de) | 1986-10-16 |
| BR7402533D0 (pt) | 1974-12-03 |
| AU6738874A (en) | 1975-10-02 |
| IT1003928B (it) | 1976-06-10 |
| SE419641B (sv) | 1981-08-17 |
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