IP Library Granted Patent US 11,358,924
Granted Patent B2
US 11,358,924 · App. 15/982,625 · Granted Jun 14, 2022

Dissociation of a 1,4-bis (4-phenoxybenzoyl)benzene-lewis acid complex in an aqueous solution

Inventors: Guillaume Le (Hérouville Saint Clair, FR); Julien Jouanneau (Corneville sur Risle, FR)
Assignee: ARKEMA FRANCE
C07C45/46C07C45/79C07C45/80C07C45/85C08G61/127C08G65/4012C08G65/4093C07C49/84C08G2261/3442C08G2261/45C08G2650/62
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Quick Facts
Patent No.
US 11,358,924
App. No.
15/982,625
Granted
Jun 14, 2022
Kind
B2
Abstract

A method for manufacturing 1,4-bis(4-phenoxybenzoyl)benzene, including: reacting terephthaloyl chloride with diphenyl ether in a reaction solvent and in the presence of a Lewis acid, so as to obtain a product mixture including a 1,4-bis(4-phenoxybenzoyl)benzene-Lewis acid complex; contacting the product mixture with an aqueous solution, so as to obtain an aqueous phase containing the Lewis acid and an organic phase containing 1,4-bis(4-phenoxybenzoyl)benzene; heating at least the second phase up to a maximum temperature, followed by cooling the second phase down to a separation temperature; subjecting at least the second phase to a solid/liquid separation step at the separation temperature, so as to recover solid 1,4-bis(4-phenoxybenzoyl)benzene.

Claims (21)

1. A method for manufacturing 1,4-bis(4-phenoxybenzoyl)benzene, comprising:

reacting terephthaloyl chloride with diphenyl ether in a reaction solvent and in the presence of a Lewis acid, so as to obtain a product mixture comprising a 1,4-bis(4-phenoxybenzoylbenzene)-Lewis acid complex, wherein the reaction solvent is ortho-dichlorobenzene and wherein the Lewis acid is aluminum trichloride; and

contacting the product mixture with an aqueous solution, so as to obtain an aqueous phase containing the Lewis acid and an organic phase containing 1,4-bis(4-phenoxybenzoyl)benzene,

wherein the concentration of Lewis acid in the product mixture is from 10 to 25%, and wherein the aqueous phase contains at least 90% of the Lewis acid from the product mixture, and wherein the relative weight ratio of product mixture and aqueous solution put in contact is from 3 to 0.5.

2. The method of claim 1 , wherein the aqueous solution has a pH of not more than 5.

3. The method of claim 1 , wherein the product mixture is poured into a vessel containing the aqueous solution.

4. The method of claim 1 , further comprising:

separating the aqueous phase from the organic phase; and/or

heating the organic phase up to a maximum temperature, followed by cooling the organic phase down to a separation temperature.

5. The method of claim 4 , wherein from 30 to 99.9 wt. % of the 1,4-bis(4-phenoxybenzoyl)benzene contained in the organic phase is dissolved in the organic phase at the maximum temperature.

6. The method of claim 4 , wherein the maximum temperature is from 90 to 150° C.

7. The method of claim 4 , wherein the separation temperature is at least 20° C.

8. The method of claim 4 , wherein the organic phase is cooled down at a rate of from 10 to 50° C./h.

9. The method of claim 1 , wherein at least the organic phase is subjected to a solid/liquid separation step so as to recover solid 1,4-bis(4-phenoxybenzoyl)benzene.

10. The method of claim 9 , wherein the solid/liquid separation step is performed at a temperature of at least 20° C.

11. The method of claim 9 , comprising one or more steps of washing the recovered solid 1,4-bis(4-phenoxybenzoyl)benzene in a protic solvent and subjecting it to a further solid/liquid separation.

12. The method of claim 11 , wherein at least one of the steps of washing the solid 1,4-bis(4-phenoxybenzoyl)benzene in a protic solvent is performed at a temperature of at least 20° C.

13. The method of claim 1 , wherein the organic phase comprises at least 50% of the 1,4-bis(4-phenoxybenzoyl)benzene in the product mixture.

14. A method of making a polyether ketone polymer, comprising:

manufacturing 1,4-bis(4-phenoxybenzoyl)benzene according to the method of claim 1 ; and

reacting said 1,4-bis(4-phenoxybenzoyl)benzene with at least one difunctional aromatic acyl chloride.

Assignments (2)
CHANGE OF ADDRESS Recorded Jul 4, 2025
From: ARKEMA FRANCE
To: ARKEMA FRANCE
Reel/Frame 071814/0739 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 18, 2018
From: LE, GUILLAUME; JOUANNEAU, JULIEN
To: ARKEMA FRANCE
Reel/Frame 045841/0605 →
Priority Claims (1)
EP 17305581 · May 18, 2017 · regional
Continuity (1)
Related Publication 20180334420A1 · Nov 22, 2018