Copper‐Promoted Oxidative Amidation of Imines: A Facile Route to Amides

Author:

Cao Zhonghua1,Sheng Da1,Zhang Zhiyang1,Ren Haitao2,Liu Yong3,Wu Songhai1,Zhang Jiaxiang4,Han Xu1ORCID

Affiliation:

1. Tianjin Key Laboratory of Chemical Process Safety and Equipment Technology School of Chemical Engineering and Technology Tianjin University Tianjin 300350 P.R. China

2. School of Textile Science and Engineering Tiangong University Tianjin 300387 P. R. China

3. School of Chemistry and Chemical Engineering Tianjin University of Technology Tianjin 300384 P.R. China

4. Key Laboratory for Green Chemical Technology of the Ministry of Education School of Chemical Engineering and Technology Tianjin University Tianjin 300072 P.R. China

Abstract

AbstractHerein, an environmentally friendly and efficient amidation method of imines by Oxone and CuO has been developed. This facile method shows excellent selectivity without affecting other functional groups such as phenyls, halogens, cyans, esters or heterocycles. This method features a broad substrate scope, mild conditions and high yields (≤90 %), and the yield in the gram scale experiment also reaches up to 81 %. Flonicamid, moclobemide and bupivacaine are also successfully synthesized to demonstrate its potential utilities.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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