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使用卤化四烷基铵作为氧化还原催化剂对苯并恶唑进行电化学引发的氧化胺化反应。

Electrochemically initiated oxidative amination of benzoxazoles using tetraalkylammonium halides as redox catalysts.

作者信息

Gao Wei-Jing, Li Wei-Cui, Zeng Cheng-Chu, Tian Hong-Yu, Hu Li-Ming, Little R Daniel

机构信息

College of Life Science & Bioengineering, Beijing University of Technology , Beijing 100124, China.

出版信息

J Org Chem. 2014 Oct 17;79(20):9613-8. doi: 10.1021/jo501736w. Epub 2014 Oct 6.

Abstract

An electrochemically promoted coupling of benzoxazoles and amines has been developed, leading directly to the formation of 2-aminobenzoxazoles. The chemistry utilizes catalytic quantities of a tetraalkylammonium halide redox catalyst and is carried out under constant current conditions in a simple undivided cell. The use of excess chemical oxidant or large amounts of supporting electrolyte is avoided. This greatly simplifies the workup and isolation process and leads to a reduction in waste.

摘要

已开发出一种电化学促进的苯并恶唑与胺的偶联反应,可直接生成2-氨基苯并恶唑。该化学方法利用催化量的四烷基卤化铵氧化还原催化剂,并在简单的无隔膜电池中恒流条件下进行。避免了使用过量的化学氧化剂或大量的支持电解质。这极大地简化了后处理和分离过程,并减少了废物产生。

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