IP Library Granted Patent US 9,982,002
Granted Patent B2
US 9,982,002 · App. 15/029,945 · Granted May 29, 2018

Sulfoxidation catalysts and methods for their preparation and use

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Quick Facts
Patent No.
US 9,982,002
App. No.
15/029,945
Granted
May 29, 2018
Kind
B2
Abstract

Methods and compositions of catalysts for sulfoxidation reaction processes are disclosed. The sulfoxidation reaction process can be performed in an aqueous medium, and the catalysts can be recycled for further use. In some embodiments, a method of making a catalyst may include contacting a transition metal compound with an oxidizing agent to form a first solution, contacting a carboxylic acid compound with a cationic surfactant to form a second solution, mixing the first solution and the second solution to form a precipitate, and isolating the precipitate.

Claims (37)

1. A method of making a catalyst of formula I:

wherein Z is alkylene, arylene, alkenylene, or alkynylene;

R 1 is alkyl, aryl, alkenyl, or alkynyl;

R 2 is alkyl, aryl, alkenyl, or alkynyl;

R 3 is alkyl, aryl, alkenyl, or alkynyl;

n is an integer from 1 to 20; and

X is Mo, V, or Cr, the method comprising:

contacting a transition metal compound with an oxidizing agent to form a first solution;

contacting a carboxylic acid compound with a cationic surfactant to form a second solution;

mixing the first solution and the second solution to form a precipitate; and

isolating the catalyst.

2. The method of claim 1 , wherein contacting the transition metal compound comprises contacting a molybdate compound, a vanadate compound, or a chromate compound.

3. The method of claim 1 , wherein contacting the carboxylic acid compound comprises contacting oxalic acid, malonic acid, benzoic acid, a pyridine carboxylic acid, lactic acid, maleic acid, succinic acid, glutaric acid, adipic acid, pimelic acid, azelaic acid, sebacic acid, fumaric acid, or any combination thereof.

4. The method of claim 1 , wherein contacting the transition metal compound with the oxidizing agent comprises contacting with potassium persulfate, ammonium persulfate, hydrogen peroxide, benzoyl peroxide, di-tert-butyl peroxide, decanoyl peroxide, lauroyl peroxide, perbenzoic acid, peracetic acid, performic acid, monoperphthalic acid, or any combination thereof.

5. The method of claim 1 , wherein contacting the carboxylic acid compound with the cationic surfactant comprises contacting with dimethyl dioctadecyl ammonium chloride, alkyldimethylbenzyl ammonium chloride, cetyltrimethyl ammonium bromide, cetyltrimethyl ammonium chloride, benzethonium chloride, or any combination thereof.

6. The method of claim 1 , wherein contacting the transition metal compound with the oxidizing agent comprises contacting the transition metal compound with the oxidizing agent in a molar ratio of 1:10 to 1:20.

7. The method of claim 1 , wherein contacting the transition metal compound with the oxidizing agent comprises contacting the transition metal compound with the oxidizing agent to form a solution having a pH of 1 to 4.

8. The method of claim 1 , wherein contacting the carboxylic acid compound with the cationic surfactant comprises contacting the carboxylic acid compound with the cationic surfactant in a molar ratio of 1:1 to 1:3.

9. The method of claim 1 , further comprising maintaining acidity below a pH of 4 during mixing the first solution and the second solution.

10. A sulfoxidation process comprising:

contacting a sulfide with a catalyst of formula I

wherein Z is alkylene, arylene, alkenylene, or alkynylene;

R 1 is alkyl, aryl, alkenyl, or alkynyl;

R 2 is alkyl, aryl, alkenyl, or alkynyl;

R 3 is alkyl, aryl, alkenyl, or alkynyl;

n is an integer from 1 to 20; and

X is Mo, V, or Cr, to form a first reaction mixture;

contacting an oxidizing agent with the first reaction mixture to form a second reaction mixture; and

isolating a product from the second reaction mixture.

11. The method of claim 10 , wherein contacting the sulfide comprises contacting an alkyl sulfide, an aryl sulfide, a substituted aryl sulfide, a cyclic alkyl sulfide, or a combination thereof.

12. The method of claim 10 , wherein contacting the oxidizing agent comprises contacting potassium persulfate, ammonium persulfate, hydrogen peroxide, benzoyl peroxide, di-tert-butyl peroxide, decanoyl peroxide, lauroyl peroxide, perbenzoic acid, peracetic acid, performic acid, monoperphthalic acid, or any combination thereof.

13. The method of claim 10 , wherein contacting the oxidizing agent comprises contacting with the sulfide present in the second reaction mixture at a concentration of 30 mole percent to 60 mole percent.

14. The method of claim 10 , wherein contacting the oxidizing agent comprises contacting with the catalyst present in the second reaction mixture at a concentration of 1 mole percent to 10 mole percent.

15. The method of claim 10 , wherein the oxidizing agent is present in the second reaction mixture at a concentration of 40 mole percent to 60 mole percent.

16. The method of claim 10 , wherein isolating the product comprises adding at least one organic solvent to the second reaction mixture.

17. The method of claim 16 , wherein isolating the product further comprises removing the solvent from the second reaction mixture.

18. The method of claim 10 , wherein isolating the product comprises isolating at least one sulfoxide, at least one sulfone, or any combination thereof.

Assignments (3)
RELEASE OF SECURITY INTEREST Recorded Jul 31, 2019
From: CRESTLINE DIRECT FINANCE, L.P.
To: EMPIRE TECHNOLOGY DEVELOPMENT LLC
Reel/Frame 049924/0794 →
SECURITY INTEREST Recorded Jan 29, 2019
From: EMPIRE TECHNOLOGY DEVELOPMENT LLC
To: CRESTLINE DIRECT FINANCE, L.P.
Reel/Frame 048373/0217 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 15, 2016
From: CHAND, DILLIP KUMAR; CHAKRAVARTHY, RAJAN DEEPAN
To: INDIAN INSTITUTE OF TECHNOLOGY MADRAS
Reel/Frame 038295/0910 →