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-氨基偶氮苯的电化学环化反应:醛类在N-N键断裂中的作用

Electrochemical Cyclization of -Aminyl Azobenzenes: Roles of Aldehydes in N-N Bond Cleavage.

作者信息

Li Anni, Gao Anna, Chen Kangjia, Li Hongji

机构信息

Key Laboratory of Green and Precise Synthetic Chemistry, Ministry of Education, School of Chemistry and Materials Science, Huaibei Normal University, Huaibei, Anhui 235000, P. R. China.

出版信息

Org Lett. 2024 Aug 2;26(30):6324-6329. doi: 10.1021/acs.orglett.4c01828. Epub 2024 Jul 22.

Abstract

Direct functionalization of azobenzenes provides an approach to obtaining valuable molecules in synthetic chemistry. However, an efficient method for the cleavage of the N═N bond of azobenzenes, which is a key process for this transformation, is still lacking. We herein disclose an electrochemical reduction-induced cyclization of azobenzenes with aldehydes via N═N bond cleavage. This electrochemical cyclization of azobenzenes proceeds well in the absence of any transition metals or external chemical oxidants, leading to the formation of N-protected benzimidazoles in moderate to good yields.

摘要

偶氮苯的直接官能团化提供了一种在合成化学中获得有价值分子的方法。然而,仍然缺乏一种有效的方法来裂解偶氮苯的N═N键,而这是该转化的关键过程。我们在此公开了一种通过N═N键裂解实现的电化学还原诱导的偶氮苯与醛的环化反应。这种偶氮苯的电化学环化反应在没有任何过渡金属或外部化学氧化剂的情况下顺利进行,以中等至良好的产率生成N-保护的苯并咪唑。

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