MX2019013003A - Disociacion de un complejo de 1,4-bis(4-fenoxibenzoil)benceno-acid o de lewis en una solucion acuosa. - Google Patents
Disociacion de un complejo de 1,4-bis(4-fenoxibenzoil)benceno-acid o de lewis en una solucion acuosa.Info
- Publication number
- MX2019013003A MX2019013003A MX2019013003A MX2019013003A MX2019013003A MX 2019013003 A MX2019013003 A MX 2019013003A MX 2019013003 A MX2019013003 A MX 2019013003A MX 2019013003 A MX2019013003 A MX 2019013003A MX 2019013003 A MX2019013003 A MX 2019013003A
- Authority
- MX
- Mexico
- Prior art keywords
- phenoxybenzoylbenzene
- bis
- lewis acid
- aqueous solution
- dissociation
- 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 4
- 239000002841 Lewis acid Substances 0.000 title abstract 4
- 239000007864 aqueous solution Substances 0.000 title abstract 2
- 238000010494 dissociation reaction Methods 0.000 title 1
- 230000005593 dissociations Effects 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 2
- 150000007517 lewis acids Chemical class 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 239000008346 aqueous phase Substances 0.000 abstract 1
- 239000007810 chemical reaction solvent Substances 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000012074 organic phase Substances 0.000 abstract 1
- LXEJRKJRKIFVNY-UHFFFAOYSA-N terephthaloyl chloride Chemical compound ClC(=O)C1=CC=C(C(Cl)=O)C=C1 LXEJRKJRKIFVNY-UHFFFAOYSA-N 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
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/78—Separation; Purification; Stabilisation; Use of additives
- C07C45/79—Separation; Purification; Stabilisation; Use of additives by solid-liquid treatment; by chemisorption
-
- 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
- C07C45/78—Separation; Purification; Stabilisation; Use of additives
- C07C45/80—Separation; Purification; Stabilisation; Use of additives by liquid-liquid treatment
-
- 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
- C07C45/78—Separation; Purification; Stabilisation; Use of additives
- C07C45/85—Separation; Purification; Stabilisation; Use of additives by treatment giving rise to a chemical modification
-
- 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
-
- 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
- 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
- C08G65/4093—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 characterised by the process or apparatus used
-
- 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
- C08G2650/28—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterised by the polymer type
- C08G2650/38—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterised by the polymer type containing oxygen in addition to the ether group
- C08G2650/40—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterised by the polymer type containing oxygen in addition to the ether group containing ketone groups, e.g. polyarylethylketones, PEEK or PEK
-
- 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)
- General Chemical & Material Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Polyethers (AREA)
Abstract
La invención se refiere a un método para manufacturar 1,4-bis(4-fenoxibenzoilbenceno), que comprende: -reaccionar cloruro de tereftaloilo con difenil éter en un solvente de reacción y en la presencia de un ácido de Lewis, para obtener una mezcla de producto que comprende un complejo de 1,4-bis(4-fenoxibenzoilbenceno)-ácido de Lewis; - poner en contacto la mezcla del producto con una solución acuosa, para obtener una fase acuosa que contenga el ácido de Lewis y una fase orgánica que contenga 1,4-bis(4-fenoxibenzoilbenceno).
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP17305581.5A EP3404011B1 (en) | 2017-05-18 | 2017-05-18 | Dissociation of a 1,4-bis(4-phenoxybenzoyl)benzene-lewis acid-complex in an aqueous solution |
| PCT/EP2018/063013 WO2018211045A1 (en) | 2017-05-18 | 2018-05-17 | Dissociation of a 1,4-bis (4-phenoxybenzoylbenzene) - lewis acid complex in an aqueous solution |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX2019013003A true MX2019013003A (es) | 2020-02-05 |
Family
ID=58779047
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2019013003A MX2019013003A (es) | 2017-05-18 | 2018-05-17 | Disociacion de un complejo de 1,4-bis(4-fenoxibenzoil)benceno-acid o de lewis en una solucion acuosa. |
Country Status (11)
| Country | Link |
|---|---|
| US (2) | US11358924B2 (es) |
| EP (2) | EP3404011B1 (es) |
| JP (1) | JP6795711B2 (es) |
| KR (1) | KR102196909B1 (es) |
| CN (1) | CN110650938A (es) |
| BR (1) | BR112019023478A2 (es) |
| CA (1) | CA3061558A1 (es) |
| ES (1) | ES2829267T3 (es) |
| MX (1) | MX2019013003A (es) |
| RU (1) | RU2019141830A (es) |
| WO (1) | WO2018211045A1 (es) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| EP3404008B1 (en) | 2017-05-16 | 2020-08-12 | Arkema France | Method for manufacturing 1,4-bis (4-phenoxybenzoyl)benzene at an elevated temperature |
| 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 |
| EP3404012B1 (en) | 2017-05-18 | 2020-09-09 | Arkema France | Ripening of 1,4-bis (4-phenoxybenzoyl)benzene |
| 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 |
| 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 |
Family Cites Families (30)
| 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 |
| SU626555A1 (ru) | 1973-03-05 | 1979-07-25 | Институт высокомолекулярных соединений | 1,4 Бис (4-ацетил-4-феноксибензоил) бензол-мономер дл прочного при изгибе и термостойкого полимера |
| SU638588A1 (ru) | 1977-06-28 | 1978-12-25 | Ярославский политехнический институт | Способ получени 1,4-бис(4 -феноксибензоил)-бензола |
| US4709007A (en) * | 1983-03-31 | 1987-11-24 | Raychem Corporation | Preparation of aromatic polymers |
| 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 |
| CA1246297A (en) * | 1985-03-11 | 1988-12-06 | Robert A. Clendinning | Process for preparing poly(aryl ether ketones) |
| US4891167A (en) * | 1985-05-02 | 1990-01-02 | Amoco Corporation | Block polymers containing a poly(aryl ether ketone) and methods for their production |
| US4704448A (en) * | 1985-11-25 | 1987-11-03 | E. I. Du Pont De Nemours And Company | Copolyetherketones |
| US5137988A (en) * | 1986-07-25 | 1992-08-11 | Amoco Corporation | Amino-terminated poly(aryl ether ketones) |
| 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 |
| JPH04103517A (ja) | 1990-08-22 | 1992-04-06 | Lion Corp | 毛髪化粧料 |
| US5258491A (en) * | 1992-09-04 | 1993-11-02 | Eastman Kodak Company | Process for preparation of a polyetherketone |
| GB9403944D0 (en) | 1994-03-02 | 1994-04-20 | Victrex Manufacturing Ltd | Aromatic polymers |
| FR2993567B1 (fr) * | 2012-07-20 | 2015-09-25 | Arkema France | Procede de synthese de poly-aryl-ether-cetones |
| 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 |
| EP3404012B1 (en) | 2017-05-18 | 2020-09-09 | Arkema France | Ripening of 1,4-bis (4-phenoxybenzoyl)benzene |
| 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 |
| EP3404013B1 (en) * | 2017-05-18 | 2021-10-27 | Arkema France | Purification of 1,4-bis (4-phenoxybenzoyl)benzene by centrifugal filtration |
| EP3404008B1 (en) | 2017-05-16 | 2020-08-12 | Arkema France | Method for manufacturing 1,4-bis (4-phenoxybenzoyl)benzene at an elevated temperature |
| 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 |
| EP3404009B1 (en) | 2017-05-16 | 2019-12-25 | Arkema France | Method for manufacturing 1,4-bis(4-phenoxybenzoyl)benzene in supersaturation conditions |
| EP3438085A1 (en) * | 2017-08-04 | 2019-02-06 | Arkema France | Process for producing polyether ketone ketone |
| EP3650434A1 (en) | 2018-11-09 | 2020-05-13 | Arkema France | Method for manufacturing 1,4-bis (4-phenoxybenzoylbenzene) using substantially non-hydrolyzed terephthaloyl chloride |
-
2017
- 2017-05-18 EP EP17305581.5A patent/EP3404011B1/en active Active
- 2017-05-18 ES ES17305581T patent/ES2829267T3/es active Active
-
2018
- 2018-05-17 KR KR1020197036781A patent/KR102196909B1/ko active Active
- 2018-05-17 US US15/982,625 patent/US11358924B2/en active Active
- 2018-05-17 BR BR112019023478-0A patent/BR112019023478A2/pt not_active Application Discontinuation
- 2018-05-17 CA CA3061558A patent/CA3061558A1/en not_active Abandoned
- 2018-05-17 US US16/613,600 patent/US20200109100A1/en not_active Abandoned
- 2018-05-17 CN CN201880032786.1A patent/CN110650938A/zh active Pending
- 2018-05-17 EP EP18724254.0A patent/EP3625205A1/en not_active Withdrawn
- 2018-05-17 MX MX2019013003A patent/MX2019013003A/es unknown
- 2018-05-17 JP JP2019563519A patent/JP6795711B2/ja not_active Expired - Fee Related
- 2018-05-17 RU RU2019141830A patent/RU2019141830A/ru not_active Application Discontinuation
- 2018-05-17 WO PCT/EP2018/063013 patent/WO2018211045A1/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| RU2019141830A (ru) | 2021-06-18 |
| EP3625205A1 (en) | 2020-03-25 |
| US20180334420A1 (en) | 2018-11-22 |
| RU2019141830A3 (es) | 2021-06-18 |
| CN110650938A (zh) | 2020-01-03 |
| US20200109100A1 (en) | 2020-04-09 |
| EP3404011A1 (en) | 2018-11-21 |
| ES2829267T3 (es) | 2021-05-31 |
| US11358924B2 (en) | 2022-06-14 |
| EP3404011B1 (en) | 2020-08-26 |
| KR102196909B1 (ko) | 2020-12-30 |
| KR20200003203A (ko) | 2020-01-08 |
| CA3061558A1 (en) | 2018-11-22 |
| JP2020520361A (ja) | 2020-07-09 |
| BR112019023478A2 (pt) | 2020-06-30 |
| WO2018211045A1 (en) | 2018-11-22 |
| JP6795711B2 (ja) | 2020-12-02 |
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