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:
Aug. 18, 2020

Filed:

Mar. 09, 2020
Applicants:

Zhejiang Zhongxin Fluoride Materials Co., Ltd., Shaoxing, CN;

Shaoxing Zhongke Baiyun Chemical Technology Co., Ltd., Shaoxing, CN;

Inventors:

Qiliang Yuan, Shaoxing, CN;

Jie Qian, Shaoxing, CN;

Xin Lai, Shaoxing, CN;

Haifeng Chen, Shaoxing, CN;

Yinhao Chen, Shaoxing, CN;

Chao Wang, Shaoxing, CN;

Assignee:

Other;

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
C07C 209/48 (2006.01); C07C 209/74 (2006.01); B01J 21/18 (2006.01); B01J 31/28 (2006.01); B01J 23/44 (2006.01); C07C 255/50 (2006.01); C07C 211/29 (2006.01);
U.S. Cl.
CPC ...
C07C 209/48 (2013.01); B01J 21/18 (2013.01); B01J 23/44 (2013.01); B01J 31/28 (2013.01); C07C 209/74 (2013.01); C07C 255/50 (2013.01); C07C 211/29 (2013.01);
Abstract

The disclosure provides a synthesis method of 2,4,6-trifluorobenzylamine, belonging to the technical field of chemical synthesis. The synthesis method is characterized by comprising the following steps: (1) allowing pentachlorobenzonitrile as a raw material to undergo fluoridation reaction with a fluoridation agent based on 2,4,6-trifluoro-3,5-dichlorobenzonitrile as a solvent to obtain 2,4,6-trifluoro-3,5-dichlorobenzonitrile; (2) hydrogenating the obtained 2,4,6-trifluoro-3,5-dichlorobenzonitrile with hydrogen in the presence of organic carboxylic acid, based, on palladium carbon as a catalyst to obtain 2,4,6-trifluoro-3,5-dichlorobenzylamine; and (3) hydrogenating the obtained 2,4,6-trifluoro-3,5-dichlorobenzylamine with hydrogen in a solvent in the presence of a catalyst to obtain 2,4,6-trifluorobenzylamine. The synthesis method has the advantages of low raw material cost, short reaction steps, high reaction yield, good product purity simple operation and the like, and is suitable for industrial production.


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