IP Library Granted Patent US 7,514,524
Granted Patent B2
US 7,514,524 · App. 11/694,405 · Granted Apr 7, 2009

Methods for producing and purifying 2-hydrocarbyl-3,3-bis(4-hydroxyaryl)phthalimidine monomers and polycarbonates derived therefrom

Assignee: SABIC Innovative Plastics IP B.V.
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Quick Facts
Patent No.
US 7,514,524
App. No.
11/694,405
Granted
Apr 7, 2009
Kind
B2
Abstract

Disclosed herein is a method comprising reacting a phenolphthalein material and a primary hydrocarbyl amine in the presence of an acid catalyst to form a reaction mixture comprising 2-hydrocarbyl-3,3-bis(4-hydroxyaryl)phthalimidine, wherein the phenolphthalein material comprises greater than or equal to 95 weight percent phenolphthalein, based on the total weight of phenolphthalein material; quenching the reaction mixture and treating the quenched reaction mixture to obtain a first solid. The first solid is then triturated with a trituration solvent and washed to obtain a second solid, wherein the second solid comprises greater than or equal to 97 weight percent 2-hydrocarbyl-3,3-bis(4-hydroxyaryl)phthalimidine, based on the total weight of the second solid. The second solid may be polymerized to form a polycarbonate.

Claims (46)

1. A method comprising:

reacting a phenolphthalein material and a primary hydrocarbyl amine in the presence of an acid catalyst to form a reaction mixture comprising 2-hydrocarbyl-3,3-bis(4-hydroxyaryl)phthalimidine, wherein the phenolphthalein material comprises greater than or equal to 95 weight percent phenolphthalein, based on the total weight of phenolphthalein material;

quenching the reaction mixture;

treating the quenched reaction mixture to obtain a first solid;

triturating the first solid with a triturating solvent and washing to obtain a second solid, wherein the second solid comprises greater than or equal to 97 weight percent 2-hydrocarbyl-3,3-bis(4-hydroxyaryl)phthalimidine, based on the total weight of the second solid; and

wherein the 2-hydrocarbyl-3,3-bis(4-hydroxyaryl)phthalimidine has a formula of:

wherein R 1 is selected from the group consisting of a hydrogen, and a hydrocarbyl group, and R 2 is selected from the group consisting of a hydrogen, a hydrocarbyl group, and a halogen.

2. The method of claim 1 wherein quenching is performed with an acid and forms a slurry comprising a precipitate and treating the quenched reaction mixture comprises:

filtering the slurry to isolate the precipitate; and

washing the precipitate with water to obtain a washed precipitate, wherein the water has a temperature of 25 to 90° C. to obtain the first solid.

3. The method of claim 2 , wherein the acid used in quenching is aqueous hydrochloric acid.

4. The method of claim 1 , wherein the quenching is performed with aqueous base and forms a biphasic system and treating the quenched reaction mixture comprises:

adding an organic solvent to the biphasic system;

removing the basic layer of the biphasic system after adding the organic solvent;

acidifying the basic layer and forming a first solid; and

isolating the first solid.

5. The method of claim 4 , wherein the basic layer is treated with an adsorbent prior to acidification.

6. The method of claim 1 , wherein the phenolphthalein material comprises greater than or equal to 97 weight percent phenolphthalein, based on the total weight of the phenolphthalein material.

7. The method of claim 1 , wherein the phenolphthalein material and the primary hydrocarbyl amine are reacted at a temperature of 140° C. to 180° C. for 8 to 50 hours.

8. The method of claim 1 , wherein the acid catalyst is selected from the group consisting of hydrochloric acid, sulfuric acid, nitric acid, phosphoric acid, boric acid, organic sulfonic acids, stannic chloride, aluminum trichloride, zinc dichloride; sulfated zirconia, and combinations of two or more of the foregoing acid catalysts.

9. The method of claim 1 , wherein the catalyst is hydrochloric acid.

10. The method of claim 1 , wherein the triturating solvent is a methanol:water mixture.

11. The method of claim 1 , wherein the primary hydrocarbyl amine is aniline.

12. The method of claim 11 , wherein the second solid comprises 2-phenyl-3,3-bis(4-hydroxphenyl)phthalimidine.

13. The method of claim 1 , wherein the second solid comprises greater than or equal to 99 weight percent 2-hydrocarbyl-3,3-bis(4-hydroxyaryl)phthalimidine, based on the total weight of the second solid.

14. The method of claim 1 , wherein the second solid is polymerizable.

15. The method of claim 1 , wherein the second solid comprises less than or equal to 50 parts per million by weight of residual solvent based on the total weight of the second solid.

16. The method of claim 1 , wherein the second solid comprises less than or equal to 1000 parts per million by weight of phenolphthalein based on the total weight of the second solid.

17. The method of claim 16 , wherein the second solid comprises less than or equal to 500 parts per million by weight of phenolphthalein based on the total weight of the second solid.

18. A method of making a polycarbonate comprising:

reacting a phenolphthalein material and a primary hydrocarbyl amine in the presence of an acid catalyst to form a reaction mixture comprising 2-hydrocarbyl-3,3-bis(4-hydroxyaryl)phthalimidine, wherein the phenolphthalein material comprises greater than or equal to 95 weight percent phenolphthalein, based on the total weight of phenolphthalein material;

quenching the reaction mixture;

treating the quenched mixture to obtain a first solid;

triturating the first solid with a triturating solvent and washing the solid after trituration to obtain a second solid wherein the second solid comprises greater than or equal to 97 weight percent 2-hydrocarbyl-3,3-bis(4-hydroxyaryl)phthalimidine, based on the total weight of the second solid; and wherein the 2-hydrocarbyl-3,3-bis(4-hydroxyaryl)phthalimidine has a formula of:

 wherein R 1 is selected from the group consisting of a hydrogen, and a hydrocarbyl group, and R 2 is selected from the group consisting of a hydrogen, a hydrocarbyl group, and a halogen; and

polymerizing the third solid to form a polycarbonate.

19. The method of claim 18 , wherein polymerizing the second solid comprises interfacial polymerization or melt polymerization.

20. The method of claim 18 , wherein quenching is performed with an acid and forms a slurry comprising a precipitate and treating the quenched reaction mixture comprises:

filtering the slurry to isolate the precipitate; and

washing the precipitate with water to obtain a washed precipitate, wherein the water has a temperature of 25 to 90° C. to obtain the first solid.

21. The method of claim 20 , wherein the acid used in quenching is aqueous hydrochloric acid.

22. The method of claim 18 , wherein the quenching is performed with aqueous base and forms a biphasic system and treating the quenched reaction mixture comprises:

adding an organic solvent to the biphasic system;

removing the basic layer of the biphasic system after adding the organic solvent;

acidifying the basic layer and forming a first solid; and

isolating the first solid.

Assignments (7)
CORRECTIVE ASSIGNMENT TO CORRECT THE REMOVE THE APPLICATION NUMBER 15039474 PREVIOUSLY RECORDED AT REEL: 054528 FRAME: 0467. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Mar 23, 2021
From: SABIC GLOBAL TECHNOLOGIES B.V.
To: SHPP GLOBAL TECHNOLOGIES B.V.
Reel/Frame 057453/0680 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 26, 2020
From: SABIC GLOBAL TECHNOLOGIES B.V.
To: SHPP GLOBAL TECHNOLOGIES B.V.
Reel/Frame 054528/0467 →
CHANGE OF NAME Recorded Jun 6, 2016
From: SABIC INNOVATIVE PLASTICS IP B.V.
To: SABIC GLOBAL TECHNOLOGIES B.V.
Reel/Frame 038883/0827 →
RELEASE OF SECURITY INTEREST Recorded Mar 17, 2014
From: CITIBANK, N.A.
To: SABIC INNOVATIVE PLASTICS IP B.V.
Reel/Frame 032459/0798 →
SECURITY AGREEMENT Recorded Aug 18, 2008
From: SABIC INNOVATIVE PLASTICS IP B.V.
To: CITIBANK, N.A., AS COLLATERAL AGENT
Reel/Frame 021423/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 1, 2008
From: GENERAL ELECTRIC COMPANY
To: SABIC INNOVATIVE PLASTICS IP B.V.
Reel/Frame 020985/0551 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 7, 2007
From: BASALE, RAJSHEKHAR; GANESAN, BALAKRISHNAN; GANAPATHY BHOLTA, VANKATA RAMA NARAYANAN; KISHAN, GURRAM; KULKARNI, SURENDRA; NADKARNI, PRADEEP; SHANMUGAM, SURESH; SINGH, RAVINDRA VIKRAM
To: GENERAL ELECTRIC COMPANY
Reel/Frame 019395/0615 →
Continuity (1)
Related Publication 20080242829A1 · Oct 2, 2008