MX2019012999A - Metodo para fabricar 1,4-bis(4-fenoxibenzoil)benceno en condiciones de supersaturacion. - Google Patents
Metodo para fabricar 1,4-bis(4-fenoxibenzoil)benceno en condiciones de supersaturacion.Info
- Publication number
- MX2019012999A MX2019012999A MX2019012999A MX2019012999A MX2019012999A MX 2019012999 A MX2019012999 A MX 2019012999A MX 2019012999 A MX2019012999 A MX 2019012999A MX 2019012999 A MX2019012999 A MX 2019012999A MX 2019012999 A MX2019012999 A MX 2019012999A
- Authority
- MX
- Mexico
- Prior art keywords
- phenoxybenzoylbenzene
- bis
- lewis acid
- manufacturing
- solvent
- Prior art date
Links
- ITVUPWDTDWMACZ-UHFFFAOYSA-N (4-phenoxyphenyl)-phenylmethanone Chemical compound C=1C=C(OC=2C=CC=CC=2)C=CC=1C(=O)C1=CC=CC=C1 ITVUPWDTDWMACZ-UHFFFAOYSA-N 0.000 title abstract 5
- 238000004519 manufacturing process Methods 0.000 title abstract 2
- 238000000034 method Methods 0.000 title 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 abstract 6
- 239000002841 Lewis acid Substances 0.000 abstract 4
- 239000002904 solvent Substances 0.000 abstract 3
- LXEJRKJRKIFVNY-UHFFFAOYSA-N terephthaloyl chloride Chemical compound ClC(=O)C1=CC=C(C(Cl)=O)C=C1 LXEJRKJRKIFVNY-UHFFFAOYSA-N 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 2
- 150000007517 lewis acids Chemical class 0.000 abstract 1
- 239000000376 reactant Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/45—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by condensation
- C07C45/46—Friedel-Crafts reactions
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
- C07C49/84—Ketones containing a keto group bound to a six-membered aromatic ring containing ether groups, groups, groups, or groups
-
- 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
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
- C08G61/127—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from carbon dioxide, carbonyl halide, carboxylic acids or their derivatives
-
- 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/34—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
- C08G65/38—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols
- C08G65/40—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols from phenols (I) and other compounds (II), e.g. OH-Ar-OH + X-Ar-X, where X is halogen atom, i.e. leaving group
- C08G65/4012—Other compound (II) containing a ketone group, e.g. X-Ar-C(=O)-Ar-X for polyetherketones
-
- 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
- C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G2261/30—Monomer units or repeat units incorporating structural elements in the main chain
- C08G2261/34—Monomer units or repeat units incorporating structural elements in the main chain incorporating partially-aromatic structural elements in the main chain
- C08G2261/344—Monomer units or repeat units incorporating structural elements in the main chain incorporating partially-aromatic structural elements in the main chain containing heteroatoms
- C08G2261/3442—Polyetherketones
-
- 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
- C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G2261/40—Polymerisation processes
- C08G2261/45—Friedel-Crafts-type
-
- 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
- C08G2650/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G2650/62—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterised by the nature of monomer used
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Polyethers (AREA)
Abstract
La invención se refiere a un método para fabricar 1,4-bis(4-fenoxibenzoil)benceno, que comprende: proporcionar una mezcla reactante que comprende cloruro de tereftaloilo, difenil éter y un ácido de Lewis en un solvente; reaccionar cloruro de tereftaloilo con difenil éter, para obtener una mezcla de producto que comprende un complejo de 1,4-bis(4-fenoxibenzoil)benc eno-ácido de Lewis; en donde el complejo de 1,4-bis(4-fenoxibenzoi l)benceno-ácido Lewis se disuelve en el solvente a una concentración en peso de 1,4-bis(4-fenoxibenzoil)benceno en el solvente que es mayor que el límite de saturación del complejo de 1,4-bis(4-fenoxibenzoil)benceno-ácido de Lewis durante por lo menos parte del paso de reacción del cloruro de tereftaloilo con difenil éter.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP17305561.7A EP3404009B1 (en) | 2017-05-16 | 2017-05-16 | Method for manufacturing 1,4-bis(4-phenoxybenzoyl)benzene in supersaturation conditions |
| PCT/EP2018/062796 WO2018210959A1 (en) | 2017-05-16 | 2018-05-16 | Method for manufacturing 1,4-bis (4-phenoxybenzoylbenzene) in supersaturation conditions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX2019012999A true MX2019012999A (es) | 2020-01-20 |
Family
ID=58779040
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2019012999A MX2019012999A (es) | 2017-05-16 | 2018-05-16 | Metodo para fabricar 1,4-bis(4-fenoxibenzoil)benceno en condiciones de supersaturacion. |
Country Status (11)
| Country | Link |
|---|---|
| US (2) | US20200087456A1 (es) |
| EP (2) | EP3404009B1 (es) |
| JP (1) | JP6795712B2 (es) |
| KR (1) | KR102097304B1 (es) |
| CN (1) | CN110621647B (es) |
| BR (1) | BR112019023201A2 (es) |
| CA (1) | CA3061431C (es) |
| ES (1) | ES2774725T3 (es) |
| MX (1) | MX2019012999A (es) |
| RU (1) | RU2019141274A (es) |
| WO (1) | WO2018210959A1 (es) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2513889A1 (en) | 2003-01-29 | 2004-08-19 | 454 Corporation | Double ended sequencing |
| EP2363205A3 (en) | 2006-01-11 | 2014-06-04 | Raindance Technologies, Inc. | Microfluidic Devices And Methods Of Use In The Formation And Control Of Nanoreactors |
| EP3404010B1 (en) | 2017-05-16 | 2020-08-12 | Arkema France | Method for manufacturing 1,4-bis (4-phenoxybenzoyl)benzene using substantially non-hydrolyzed terephthaloyl chloride |
| ES2829265T3 (es) | 2017-05-16 | 2021-05-31 | Arkema France | Método para fabricar 1,4-bis(4-fenoxibenzoil)benceno a una temperatura elevada |
| US10793500B2 (en) | 2017-05-16 | 2020-10-06 | Arkema France | Dissociation of 1,4-bis (4-phenoxybenzoyl)benzene—Lewis acid complex in a protic solvent |
| EP3404011B1 (en) | 2017-05-18 | 2020-08-26 | Arkema France | Dissociation of a 1,4-bis(4-phenoxybenzoyl)benzene-lewis acid-complex in an aqueous solution |
| EP3404012B1 (en) | 2017-05-18 | 2020-09-09 | Arkema France | Ripening of 1,4-bis (4-phenoxybenzoyl)benzene |
| EP3438085A1 (en) * | 2017-08-04 | 2019-02-06 | Arkema France | Process for producing polyether ketone ketone |
| EP3650433B1 (en) | 2018-11-09 | 2024-04-24 | Arkema France | Method for manufacturing 1,4-bis (4-phenoxybenzoylbenzene) at an elevated temperature |
| FR3110572B1 (fr) * | 2020-05-19 | 2022-10-07 | Arkema France | Dérivé de xanthène, mélanges le comprenant, procédé de fabrication et utilisations correspondants |
| KR20220028244A (ko) * | 2020-08-28 | 2022-03-08 | 한화솔루션 주식회사 | 1,4-비스(4-페녹시벤조일)벤젠을 제조하는 방법 및 이에 의해 제조된 1,4-비스(4-페녹시벤조일)벤젠 |
| EP4008742A1 (en) | 2020-12-04 | 2022-06-08 | Arkema France | Pulverulent composition based on paek(s), sintering construction process and object derived therefrom |
| CN119371297B (zh) * | 2024-12-30 | 2025-04-11 | 山东凯盛新材料股份有限公司 | 1,4-双(4-苯氧基苯甲酰基)苯的合成工艺 |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SU445643A1 (ru) | 1973-01-08 | 1974-10-05 | Институт Высокомолекулярных Соединений Ан Ссср | Способ получени 1,4-бис(4-феноксибензоил)бензола |
| US4816556A (en) | 1985-02-22 | 1989-03-28 | E. I. Du Pont De Nemours And Company | Ordered polyetherketones |
| US4716211A (en) | 1985-03-11 | 1987-12-29 | Amoco Corporation | Slurry process for producing high molecular weight crystalline polyaryletherketones |
| DE3789354T2 (de) | 1986-11-20 | 1994-08-04 | Asahi Chemical Ind | Aromatischer Polyether und Verfahren zur Herstellung eines Polyethers. |
| JPS63258923A (ja) * | 1987-04-16 | 1988-10-26 | Asahi Chem Ind Co Ltd | 芳香族ポリエ−テルケトンの製造方法 |
| US4826947A (en) | 1987-07-09 | 1989-05-02 | Raychem Corporation | Preparation of poly(arylene ether ketones) |
| US4794155A (en) * | 1987-08-26 | 1988-12-27 | The Dow Chemical Company | Process for forming arylether polymers |
| US4835319A (en) | 1987-11-09 | 1989-05-30 | E. I. Du Pont De Nemours And Company | Process for the manufacture of 1,4-bis(4-phenoxybenzoyl)benzene with a zeolite catalyst |
| US4827041A (en) * | 1988-03-10 | 1989-05-02 | E. I. Du Pont De Nemours And Company | Process for the manufacture of 1,4-bis(4-phenoxybenzoyl)benzene with a perfluorosulfonyl resin catalyst |
| US4918237A (en) | 1989-03-13 | 1990-04-17 | E. I. Du Pont De Nemours And Company | Process for the manufacture of 1,4-bis(4-phenoxybenzoyl)benzene with certain metal-containing catalysts |
| GB9403944D0 (en) | 1994-03-02 | 1994-04-20 | Victrex Manufacturing Ltd | Aromatic polymers |
| EP3404010B1 (en) * | 2017-05-16 | 2020-08-12 | Arkema France | Method for manufacturing 1,4-bis (4-phenoxybenzoyl)benzene using substantially non-hydrolyzed terephthaloyl chloride |
| US10793500B2 (en) * | 2017-05-16 | 2020-10-06 | Arkema France | Dissociation of 1,4-bis (4-phenoxybenzoyl)benzene—Lewis acid complex in a protic solvent |
-
2017
- 2017-05-16 ES ES17305561T patent/ES2774725T3/es active Active
- 2017-05-16 EP EP17305561.7A patent/EP3404009B1/en active Active
-
2018
- 2018-05-16 US US16/609,790 patent/US20200087456A1/en not_active Abandoned
- 2018-05-16 WO PCT/EP2018/062796 patent/WO2018210959A1/en not_active Ceased
- 2018-05-16 CN CN201880031934.8A patent/CN110621647B/zh active Active
- 2018-05-16 RU RU2019141274A patent/RU2019141274A/ru not_active Application Discontinuation
- 2018-05-16 BR BR112019023201A patent/BR112019023201A2/pt not_active Application Discontinuation
- 2018-05-16 CA CA3061431A patent/CA3061431C/en not_active Expired - Fee Related
- 2018-05-16 JP JP2019563523A patent/JP6795712B2/ja not_active Expired - Fee Related
- 2018-05-16 MX MX2019012999A patent/MX2019012999A/es unknown
- 2018-05-16 US US15/981,439 patent/US10428002B2/en active Active
- 2018-05-16 KR KR1020197036486A patent/KR102097304B1/ko active Active
- 2018-05-16 EP EP18724891.9A patent/EP3625206A1/en not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| ES2774725T3 (es) | 2020-07-22 |
| US20190135721A1 (en) | 2019-05-09 |
| KR20190140489A (ko) | 2019-12-19 |
| RU2019141274A (ru) | 2021-06-16 |
| EP3404009A1 (en) | 2018-11-21 |
| JP2020520363A (ja) | 2020-07-09 |
| KR102097304B1 (ko) | 2020-04-06 |
| US20200087456A1 (en) | 2020-03-19 |
| CN110621647B (zh) | 2021-05-25 |
| US10428002B2 (en) | 2019-10-01 |
| CA3061431A1 (en) | 2018-11-22 |
| RU2019141274A3 (es) | 2021-06-16 |
| JP6795712B2 (ja) | 2020-12-02 |
| BR112019023201A2 (pt) | 2020-05-19 |
| CA3061431C (en) | 2020-07-21 |
| EP3404009B1 (en) | 2019-12-25 |
| CN110621647A (zh) | 2019-12-27 |
| WO2018210959A1 (en) | 2018-11-22 |
| EP3625206A1 (en) | 2020-03-25 |
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