IP Library Granted Patent US 10,807,933
Granted Patent B2
US 10,807,933 · App. 16/613,587 · Granted Oct 20, 2020

Method for manufacturing 1,4-bis (4-phenoxybenzoyl)benzene using substantially non-hydrolyzed terephthaloyl chloride

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Quick Facts
Patent No.
US 10,807,933
App. No.
16/613,587
Granted
Oct 20, 2020
Kind
B2
Abstract

A method for manufacturing 1,4-bis(4-phenoxybenzoyl)benzene, including: providing terephthaloyl chloride, diphenyl ether, a solvent and a Lewis acid, wherein the terephthaloyl chloride is of a purity grade such that, 10 minutes after introducing it at a reference concentration of 6.5 wt. % into said solvent, at a temperature of 20° C., a solution is obtained having a turbidity of less than 500 NTU; mixing the terephthaloyl chloride, the diphenyl ether and the solvent so as to make a reactant mixture; adding the Lewis acid to the reactant mixture so as to effect the reaction of the terephthaloyl chloride with the diphenyl ether; recovering a product mixture comprising a 1,4-bis(4-phenoxybenzoyl)benzene-Lewis acid complex.

Claims (26)

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

providing terephthaloyl chloride, diphenyl ether, a solvent and a Lewis acid, wherein the terephthaloyl chloride is of a purity grade such that, 10 minutes after introducing it at a reference concentration of 6.5 wt. % into said solvent, at a temperature of 20° C., a solution is obtained having a turbidity of less than 500 NTU;

reacting terephthaloyl chloride with diphenyl ether in the solvent and in the presence of the Lewis acid; and

recovering a product mixture comprising a 1,4-bis(4-phenoxybenzoyl)benzene-Lewis acid complex.

2. The method of claim 1 , wherein the terephthaloyl chloride is of a purity grade such that:

10 minutes after introducing it at a reference concentration of 6.5 wt. % into said solvent, at a temperature of 20° C., a solution is obtained having a turbidity of less than 200 NTU.

3. The method of claim 1 , reacting terephthaloyl chloride with diphenyl ether in the solvent and in the presence of the Lewis acid comprises:

mixing the terephthaloyl chloride, the diphenyl ether and the solvent so as to make a reactant mixture; and

adding the Lewis acid to the reactant mixture so as to effect the reaction of the terephthaloyl chloride with the diphenyl ether.

4. The method of claim 3 , wherein the terephthaloyl chloride is kept in a sealed container without contact with ambient air prior to making the reactant mixture.

5. The method of claim 1 , wherein the diphenyl ether and solvent, in combination, contain less than 500 ppm by weight of water.

6. The method of claim 1 , wherein the diphenyl ether and solvent, in combination, contain from 1 to 250 ppm by weight of water.

7. The method of claim 3 , comprising a step of drying the solvent or of drying the solvent combined with the diphenyl ether prior to adding the terephthaloyl chloride to the solvent.

8. The method of claim 1 , wherein the 1,4-bis(4-phenoxybenzoyl)benzene-Lewis acid complex is dissolved in the solvent at a 1,4-bis(4-phenoxybenzoyl)benzene weight concentration in the solvent which is higher than the saturation limit of the 1,4-bis(4-phenoxybenzoyl)benzene-Lewis acid complex during at least part of the reaction of the terephthaloyl chloride with the diphenyl ether.

9. The method of claim 1 , wherein the 1,4-bis(4-phenoxybenzoyl)benzene-Lewis acid complex is dissolved in the solvent at a 1,4-bis(4-phenoxybenzoyl)benzene weight concentration which is higher by at least 5% than the saturation limit of the 1,4-bis(4-phenoxybenzoyl)benzene-Lewis acid complex, during part of the reaction of the terephthaloyl chloride with the diphenyl ether.

10. The method of claim 1 , wherein the 1,4-bis(4-phenoxybenzoyl)benzene-Lewis acid complex is dissolved in the solvent at a 1,4-bis(4-phenoxybenzoyl)benzene weight concentration of more than 5 wt. %, during part of the reaction of the terephthaloyl chloride with the diphenyl ether.

11. The method of claim 1 , wherein the 1,4-bis(4-phenoxybenzoyl)benzene-Lewis acid complex is dissolved in the solvent during at least 75% of the duration of the reaction of the terephthaloyl chloride with the diphenyl ether.

12. The method of claim 3 wherein the 1,4-bis(4-phenoxybenzoyl)benzene-Lewis acid complex is dissolved in the solvent when an amount of 1,4-bis(4-phenoxybenzoyl)benzene of 75 mol. %, relative to the initial amount of terephthaloyl chloride, is present in the reactant mixture.

13. The method of claim 1 , wherein the Lewis acid is aluminum trichloride.

14. The method of claim 1 , wherein the solvent is ortho-dichlorobenzene.

15. The method of claim 1 , comprising the additional steps of:

mixing the product mixture with a protic solvent so as to provide a product slurry;

separating 1,4-bis(4-phenoxybenzoyl)benzene from the product slurry.

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

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

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, 2020
From: LE, GUILLAUME; JOUANNEAU, JULIEN
To: ARKEMA FRANCE
Reel/Frame 052683/0445 →