IP Library Granted Patent US 7,049,471
Granted Patent B2
US 7,049,471 · App. 10/798,083 · Granted May 23, 2006

Separation of amine from a phenolic compound

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Quick Facts
Patent No.
US 7,049,471
App. No.
10/798,083
Granted
May 23, 2006
Kind
B2
Abstract

A process comprises contacting a product mixture with a base, optionally in the presence of a polyhydric alcohol, to produce a base-treated mixture and distilling the base-treated mixture in which the product mixture comprises an aromatic amine and a phenolic compound.

Claims (29)

1. A process comprising contacting a product mixture with a base, optionally in the presence of a polyhydric alcohol, to produce a base-treated mixture, introducing said base-treated mixture to a distillation apparatus, and distilling said base-treated mixture wherein said product mixture comprises an aromatic amine and a phenolic compound.

2. A process according to claim 1 wherein the molar ratio of said base to said phenolic compound is in the range of from about 1:1 to about 4:1.

3. A process according to claim 1 wherein the molar ratio of said base to said phenolic compound is in the range of from about 1:1 to about 2:1.

4. A process according to claim 1 wherein said base is lithium hydroxide, sodium hydroxide, sodium hydrosulfide, sodium bisulfide, potassium hydroxide, potassium hydrosulfide, potassium bisulfide, calcium hydroxide, magnesium hydroxide, sodium bicarbonate, sodium carbonate, sodium sulfide, sodium oxide, magnesium oxide, calcium oxide, calcium carbonate, sodium phenoxide, barium phenoxide, calcium phenoxide, tetramethylammonium hydroxide, tetraethylammonium hydroxide, tetrapropylammonium hydroxide, tetramethylammonium bisulfide, tetraethylammonium bisulfide, or combinations of any two or more thereof.

5. A process according to claim 2 wherein said base is lithium hydroxide, sodium hydroxide, sodium hydrosulfide, sodium bisulfide, potassium hydroxide, potassium hydrosulfide, potassium bisulfide, calcium hydroxide, magnesium hydroxide, sodium bicarbonate, sodium carbonate, sodium sulfide, sodium oxide, magnesium oxide, calcium oxide, calcium carbonate, sodium phenoxide, barium phenoxide, calcium phenoxide, tetramethylammonium hydroxide, tetraethylammonium hydroxide, tetrapropylammonium hydroxide, tetramethylammonium bisulfide, tetraethylammonium bisulfide, or combinations of any two or more thereof.

6. A process according to claim 3 wherein said base is potassium hydroxide, sodium hydroxide, or combinations thereof.

7. A process according to claim 1 wherein said amine is aniline, toluidines, chloroanilines, bromoanilines, iodoanilines, chlorotoluidines, bromotoluidines, iodotoluidines, benzylamine, N-benzylamine, ethylamines, fluoromethylanilines, chloromethylanilines, bromomethylanilines, or combinations of two or more thereof.

8. A process according to claim 5 wherein said amine is aniline, toluidines, chloroanilines, bromoanilines, iodoanilines, chlorotoluidines, bromotoluidines, iodotoluidines, benzylamine, N-benzylamine, ethylanilines, fluoromethylanilines, chloromethylanilines, bromomethylanilines, or combinations of two or more thereof.

9. A process according to claim 6 wherein said amine is aniline, toluidines, or combinations of two or more thereof.

10. A process according to claim 2 wherein said phenolic compound is phenol, cresols, chlorophenols, bromophenols, iodophenols, chlorotoluidines, bromotoluidines, iodotoluidines, benzylamine, N-benzylamine, ethylphenols, fluoromethylphenols, chloromethylphenols, bromomethylphenols, or combinations of two or more thereof.

11. A process according to claim 5 wherein said phenolic compound is phenol, cresols, chlorophenols, bromophenols, iodophenols, chlorotoluidines, bromotoluidines, iodotoluidines, benzylamine, N-benzylamine, ethylphenols, fluoromethylphenols, chloromethylphenols, bromomethylphenols, or combinations of two or more thereof.

12. A process according to claim 8 wherein said phenolic compound is phenol, cresols, chlorophenols, bromophenols, iodophenols, chlorotoluidines, bromotoluidines, iodotoluidines, benzylamine, N-benzylamine, ethylphenols, fluoromethylphenols, chloromethylphenols, bromomethylphenols, or combinations of two or more thereof.

13. A process according to claim 6 wherein said phenolic compound is phenol, cresols, or combinations of two or more thereof.

14. A process according to claim 8 wherein said phenolic compound is phenol, cresols, or combinations of two or more thereof.

15. A process according to claim 14 wherein said contacting is carried out in the presence ofa polyhydric alcohol, which is trimethylene glycol, triethylene glycol, glycerol, ethylene glycol, diethylene glycol, 1,2-propane diol, 1,3-propane diol, tripropylene glycol, polyethylene glycol, polypropylene glycol, or combinations of two or more thereof.

16. A process according to claim 15 wherein said polyhydric alcohol is polyethylene glycol.

17. A process comprising contacting a product mixture with a base to produce a base-treated mixture, introducing said base-treated mixture to a distillation apparatus and distilling said base-treated mixture,

wherein said product mixture comprises an aromatic amine and a phenolic compound;

the molar ratio of said base to said phenolic compound is in the range of from about 1:1 to about 4:1;

said base is lithium hydroxide, sodium hydroxide, calcium hydroxide, magnesium hydroxide, sodium bicarbonate, sodium carbonate, sodium oxide, magnesium oxide, calcium oxide, calcium carbonate, tetramethylammonium hydroxide, tetraethylammonium hydroxide, tetrapropylammonium hydroxide, tetramethylammonium bisulfide, tetraethylammonium bisulfide, or combinations of any two or more thereof; and

said amine is aniline, toluidines, chloroanilines, bromoanilines, iodoanilines, chlorotoluidines, bromotoluidines, iodotoluidines, benzylamine, N-benzylamine, ethylanilines, fluoromethylanilines, chloromethylanilines, bromomethylanilines, or combinations of two or more thereof.

18. A process according to claim 17 wherein said contacting is carried out in the presence of a polyhydric alcohol.

19. A process according to claim 17 wherein the molar ratio of said base to said phenolic compound is in the range of from about 1:1 to about 2:1; said amine is aniline, toluidines, or combinations of two or more thereof; said phenolic compound is phenol, cresols, or combinations of two or more thereof and said base is potassium hydroxide, sodium hydroxide, or combinations thereof.

20. A process according to claim 19 wherein said contacting is carried out in the presence of a polyhydric alcohol, which is trimethylene glycol, triethylene glycol, glycerol, ethylene glycol, diethylene glycol, 1,2-propane diol, 1,3-propane diol, tripropylene glycol, polyethylene glycol, polypropylene glycol, or combinations of two or more thereof.

21. A process according to claim 20 wherein said polyhydric alcohol is polyethylene glycol.

22. A process for separating o-cresol from o-toluidine in a mixture, which comprises said o-cresol and said o-toluidine, comprising contacting said mixture with potassium hydroxide to produce a base-treated mixture and distilling said base-treated mixture.

23. A process according to claim 22 wherein said process is carried out in the presence of a polyhydric alcohol.

24. A process according to claim 23 wherein said polyhydric alcohol is polyethylene glycol.

25. A process according to claim 1 wherein said contacting is carried out in the presence of a polyhydric alcohol.

Assignments (3)
RELEASE OF SECURITY INTEREST Recorded Apr 4, 2018
From: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
To: THE CHEMOURS COMPANY FC, LLC
Reel/Frame 045845/0913 →
SECURITY AGREEMENT Recorded Jun 10, 2015
From: THE CHEMOURS COMPANY FC LLC; THE CHEMOURS COMPANY TT, LLC
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 035839/0675 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 15, 2015
From: E. I. DU PONT DE NEMOURS AND COMPANY
To: THE CHEMOURS COMPANY FC, LLC
Reel/Frame 035432/0023 →