The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Nov. 06, 2012

Filed:

Jan. 12, 2007
Applicants:

Hirofumi Ii, Ube, JP;

Tomoyuki Ito, Ube, JP;

Yoshiki Kawamura, Ube, JP;

Toshiyuki Matsushita, Ube, JP;

Inventors:

Hirofumi Ii, Ube, JP;

Tomoyuki Ito, Ube, JP;

Yoshiki Kawamura, Ube, JP;

Toshiyuki Matsushita, Ube, JP;

Assignee:

Ube Industries, Ltd., Ube-Shi, JP;

Attorney:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
C07C 27/04 (2006.01); C07C 27/00 (2006.01); C07C 27/26 (2006.01); C07C 69/74 (2006.01);
U.S. Cl.
CPC ...
Abstract

A method is provided for producing highly pure 1,6-hexanediol in which the contents of impurities such as 1,4-cyclohexanediol, 1,5-hexanediol, 1,2-cyclohexanediol, 1,7-pentanediol, 1,5-pentanediol and high boiling point components are significantly reduced. The process contains the steps of (1) treating an aqueous extraction concentrate of a reaction mixture obtained by oxidation of cyclohexane with a lower alcohol to esterify monocarboxylic acids and dicarboxylic acids contained in the extract, and simultaneously removing and separating by distillation water, excess lower alcohols and carboxylic acid esters; (2) converting oligomer esters contained in the bottom liquid to carboxylic acid esters by depolymerizing the oligomer esters at a high temperature and high pressure in the presence of a lower alcohol and a catalyst; and (3) hydrogenating the carboxylic acid esters distilled off in step (1) and the carboxylic acid esters obtained in step (2) either respectively or collectively to convert to 1,6-hexanediol.


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