Methods of manufacture of 2-hydrocarbyl-3,3-bis(hydroxyaryl)phthalimidines

Patent metadata

Field	Value
Publication number	US-9822070-B2
Application number	US-201515111507-A
Country	US
Kind code	B2
Filing date	Jan 14, 2015
Priority date	Jan 14, 2014
Publication date	Nov 21, 2017
Grant date	Nov 21, 2017

Abstract

A method for the manufacture of a 2-hydrocarbyl-3,3-bis(hydroxyaryl)phthalimidine composition comprises: reacting a phthalimide with a phenol in the presence of a catalyst and optionally a solvent at an elevated temperature to form the 2-hydrocarbyl-3,3-bis(hydroxyaryl)phthalimidine composition.

First claim

What is claimed is:

1. A method for the manufacture of a 2-hydrocarbyl-3,3-bis(hydroxyaryl)phthalimidine composition, the method comprising
reacting a phthalimide of formula (2) with a phenol of formula (3)

in the presence of a catalyst and optionally a solvent at an elevated temperature to form the 2-hydrocarbyl-3,3-bis(hydroxyaryl)phthalimidine composition,
wherein the 2-hydrocarbyl-3,3-bis(hydroxyaryl)phthalimidine composition comprises a 2-hydrocarbyl-3,3-bis(hydroxyaryl)phthalimidine of formula (1)

wherein in formulas (1), (2) and (3),
R 1 is C 1-6 alkyl, C 1-6 alkoxy, or phenyl optionally substituted with 1 to 5 C 1-6 alkyls,
each occurrence of R 2 and R 3 is independently a C 1-6 alkyl, and
p and q are independently 0 to 4.

2. A method for the manufacture of a polycarbonate comprising
reacting a phthalimide of formula (2) with a phenol of formula (3)

in the presence of a catalyst and optionally a solvent at an elevated temperature to form a 2-hydrocarbyl-3,3-bis(hydroxyaryl)phthalimidine composition comprising a 2-hydrocarbyl-3,3-bis(hydroxyaryl)phthalimidine of formula (1)

and
polymerizing the 2-hydrocarbyl-3,3-bis(hydroxyaryl)phthalimidine of formula (1) and optionally a dihydroxy aromatic compound different from the 2-hydrocarbyl-3,3-bis(hydroxyaryl)phthalimidine of formula (1) to form the polycarbonate,

wherein in formulas (1), (2) and (3),
R 1 is C 1-6 alkyl, C 1-6 alkoxy, or phenyl optionally substituted with 1 to 5 C 1-6 alkyls,
each occurrence of R 2 and R 3 is independently a C 1-6 alkyl, and
p and q are independently 0 to 4.

3. The method of claim 1 , further comprising reacting an anhydride of formula (4) with an amine of formula (5)

to provide the phthalimide of formula (2), wherein
R 1 is C 1-6 alkyl, C 1-6 alkoxy, or phenyl optionally substituted with 1 to 5 C 1-6 alkyls,
each occurrence of R 2 is independently a C 1-6 alkyl, and
p is 0 to 4.

4. The method of claim 1 , wherein R 1 is phenyl or methyl.

5. The method of claim 1 , wherein the 2-hydrocarbyl-3,3-bis(hydroxyaryl)phthalimidine composition comprises a 2-phenyl-3,3-bis(4-hydroxyphenyl)phthalimidine of formula (6), a 2-phenyl-3-(4-hydroxyphenyl)-3-(2-hydroxyphenyl)phthalimidine of formula (7), or a combination thereof

optionally wherein a molar ratio of the 2-phenyl-3,3-bis(4-hydroxyphenyl)phthalimidine of formula (6) to the 2-phenyl-3-(4-hydroxyphenyl)-3-(2-hydroxyphenyl)phthalimidine of formula (7) is 95:5 to 5:95.

6. The method of claim 1 , wherein
the solvent is 1,2-dichlorobenzene; and
the 2-hydrocarbyl-3,3-bis(hydroxyaryl)phthalimidine composition comprises a 2-phenyl-3,3-bis(4-hydroxyphenyl)phthalimidine of formula (6) and a 2-phenyl-3-(4-hydroxyphenyl)-3-(2-hydroxyphenyl)phthalimidine (7)

having a molar ratio of formula (6):(7) of 95:5 to 80:20.

7. The method of claim 1 , wherein
the solvent is 1,1,2,2-tetrachloroethane; and
the 2-hydrocarbyl-3,3-bis(hydroxyaryl)phthalimidine composition comprises a 2-phenyl-3,3-bis(4-hydroxyphenyl)phthalimidine of formula (6) and a 2-phenyl-3-(4-hydroxyphenyl)-3-(2-hydroxyphenyl)phthalimidine (7)

and having a molar ratio of formula (6):(7) of 5:95 to 20:80.

8. The method of claim 5 , further comprising converting the 2-phenyl-3-(4-hydroxyphenyl)-3-(2-hydroxyphenyl)phthalimidine of formula (7) to the 2-phenyl-3,3-bis(4-hydroxyphenyl)phthalimidine of formula (6).

9. The method of claim 1 , wherein the catalyst used to form the 2-hydrocarbyl-3,3-bis(hydroxyaryl)phthalimidine of formula (1) is an acid catalyst or AlCl 3 .

10. The method of claim 1 , wherein the molar ratio of the phenol of formula (3) to the phthalimide of formula (2) is greater than 2.

11. The method of claim 1 , wherein the elevated temperature is 100° C. to 200° C.

12. The method of claim 1 , wherein the method further comprises cooling a crude product of the phthalimide of formula (2) and the phenol of formula (3) and quenching the cooled crude product by stirring with an acid and an organic solvent.

13. The method of claim 12 , wherein the acid is a mineral acid.

14. The method of claim 12 , wherein the organic solvent is at least one of diethyl ether, chloroform, methylene chloride, benzene, toluene, pentane, hexane, cyclohexane, and 1,2-dichloroethane.

15. The method of claim 12 , further comprising filtering and drying the quenched crude product to provide the 2-hydrocarbyl-3,3-bis(hydroxyaryl)phthalimidine composition.

16. The method of claim 15 , further comprising purifying the crude product by trituration, purifying the crude product using activated carbon, or a combination comprising at least one of the foregoing.

17. The method of claim 1 , wherein 2-hydrocarbyl-3,3-bis(hydroxyaryl)phthalimidine composition comprises less than 100 ppm of an amino phenol, 2-aryl-3-(aminoaryl-3-(hydroxyaryl)phthalimidine of formula (8) and less than 100 ppm of 2-phenyl-3-(4-hydroxyphenyl)-3-(2-hydroxyphenyl)phthalimidine of formula (7)

wherein
R 1 is C 1-6 alkyl, C 1-6 alkoxy, or phenyl optionally substituted with 1 to 5 C 1-6 alkyls,
each occurrence of R 2 and R 3 is independently a C 1-6 alkyl, and
p and q are each independently 0 to 4.

18. The method of claim 1 , wherein the 2-hydrocarbyl-3,3-bis(hydroxyaryl)phthalimidine composition is free of an amino phenol of formula (8) and 2-phenyl-3-(4-hydroxyphenyl)-3-(2-hydroxyphenyl)phthalimidine of formula (7)

wherein
R 1 is C 1-6 alkyl, C 1-6 alkoxy, or phenyl optionally substituted with 1 to 5 C 1-6 alkyls,
each occurrence of R 2 and R 3 is independently a C 1-6 alkyl, and
p and q are independently 0 to 4.

19. A 2-hydrocarbyl-3,3-bis(hydroxyaryl)phthalimidine composition manufactured by a method of claim 1 .

20. A polycarbonate manufactured by a method of claim 2 .

21. The 2-hydrocarbyl-3,3-bis(hydroxyaryl)phthalimidine composition of claim 19 , wherein 2-hydrocarbyl-3,3-bis(hydroxyaryl)phthalimidine composition comprises less than 100 ppm of an amino phenol, 2-aryl-3-(aminoaryl-3-(hydroxyaryl)phthalimidine of formula (8) and less than 100 ppm of 2-phenyl-3-(4-hydroxyphenyl)-3-(2-hydroxyphenyl)phthalimidine of formula (7)

wherein
R 1 is C 1-6 alkyl, C 1-6 alkoxy, or phenyl optionally substituted with 1 to 5 C 1-6 alkyls,
each occurrence of R 2 and R 3 is independently a C 1-6 alk

Assignees

• Sabic Global Technologies Bv

Inventors

• Bhotla Venkata Ramanarayanan Ganapathy
• Aluri Bhaskar Reddy
• Shubashree S

Classifications

• C08G64/12

  containing nitrogen · CPC title

• B01J27/125

  with scandium, yttrium, aluminium, gallium, indium or thallium · CPC title

• C07D209/46 Primary

  with an oxygen atom in position 1 · CPC title