Method for extracting asymmetric β-diketone compound from β-diketone compound

Patent metadata

Field	Value
Publication number	US-9284249-B2
Application number	US-201314438963-A
Country	US
Kind code	B2
Filing date	Oct 17, 2013
Priority date	Oct 29, 2012
Publication date	Mar 15, 2016
Grant date	Mar 15, 2016

Abstract

The present invention provides a method of extracting an asymmetric β-diketone compound from a β-diketone compound containing at least one symmetric β-diketone compound mixed in the asymmetric β-diketone compound, and the method includes the step (A) of adjusting a pH of a mixed solution of the β-diketone compound and water at 11.5 or more and dissolving the β-diketone compound into water to form a β-diketone compound solution and the step (B) of subsequently adjusting the pH of the β-diketone compound solution at 9.5 or less and recovering the asymmetric β-diketone compound of Chemical Formula 1 separated from the β-diketone compound solution. The present invention further includes at least either (a) a step of setting the upper limit of the pH of the mixed solution to 12.5 to form a β-diketone compound solution in the step (A) and bringing the β-diketone compound solution into contact with a hydrophobic solvent or (b) a step of setting the lower limit of the pH of the β-diketone compound solution to 8.0 in the step (B).

First claim

The invention claimed is:

1. A method of extracting an asymmetric β-diketone compound of Chemical Formula 1 from a β-diketone compound comprising at least either a symmetric β-diketone compound of Chemical Formula 2 or a symmetric β-diketone compound of Chemical Formula 3, said symmetric β-diketone compound being mixed in the asymmetric β-diketone compound, the method comprising the steps of:
(A): adjusting a pH of a mixed solution of the β-diketone compound and water 11.5 or more and dissolving the β-diketone compound into water to form a β-diketone compound solution;
(B): subsequently adjusting the pH of the β-diketone compound solution 9.5 or less and recovering the asymmetric β-diketone compound of Chemical Formula 1 separated from the β-diketone compound solution; and
at least either of:
(a): setting the upper limit of the pH of the mixed solution to 12.5 to form a β-diketone compound solution in the step (A) and bringing the β-diketone compound solution into contact with a hydrophobic solvent to thus transfer the symmetric β-diketone compound of Chemical Formula 3 into the hydrophobic solvent; or
(b): setting the lower limit of the pH of the β-diketone compound solution to 8.0 in the step (B) and separating and recovering the asymmetric β-diketone compound of Chemical Formula 1 separated from the β-diketone compound solution:

(in each chemical formula, R 1 and R 2 , which are substituents, are alkyl groups, and have a relationship of the number of carbon atoms in R 1 <the number of carbon atoms in R 2 , and R 3 is hydrogen or an alkyl group.).

2. The method of extracting an asymmetric β-diketone compound according to claim 1 , wherein a step of adjusting the pH of the mixed solution in the step (A) comprises adding a metal hydroxide to the mixed solution.

3. The method of extracting an asymmetric β-diketone compound according to claim 1 , wherein a step of adjusting the pH of the β-diketone compound solution in the step (B) comprises adding at least any of hydrochloric acid, sulfuric acid and perchloric acid to the solution.

4. The method of extracting an asymmetric β-diketone compound according to claim 1 , wherein the hydrophobic solvent which is brought into contact with the β-diketone compound solution in the step (a) is any one of pentane, hexane, heptane, petroleum ether, cyclohexane, benzene, toluene, xylene, diethyl ether, diisopropyl ether, dichloromethane and chloroform.

5. The method of extracting an asymmetric β-diketone compound according to claim 2 , wherein a step of adjusting the pH of the β-diketone compound solution in the step (B) comprises adding at least any of hydrochloric acid, sulfuric acid and perchloric acid to the solution.

6. The method of extracting an asymmetric β-diketone compound according to claim 2 , wherein the hydrophobic solvent which is brought into contact with the β-diketone compound solution in the step (a) is any one of pentane, hexane, heptane, petroleum ether, cyclohexane, benzene, toluene, xylene, diethyl ether, diisopropyl ether, dichloromethane and chloroform.

7. The method of extracting an asymmetric β-diketone compound according to claim 3 , wherein the hydrophobic solvent which is brought into contact with the β-diketone compound solution in the step (a) is any one of pentane, hexane, heptane, petroleum ether, cyclohexane, benzene, toluene, xylene, diethyl ether, diisopropyl ether, dichloromethane and chloroform.

Assignees

• Tanaka Precious Metal Ind

Inventors

• Harada Ryosuke
• SHIGETOMI Toshiyuki
• Miyazaki Satoshi
• Saito Masayuki

Classifications

• C07C45/80 Primary

  by liquid-liquid treatment · CPC title

• C07C49/12

  Ketones containing more than one keto group · CPC title

• C07C49/14

  Acetylacetone, i.e. 2,4-pentanedione · CPC title