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Direct electrochemical reductive amination between aldehydes and amines with a H/D-donor solvent†
Huanliang Hong,Zirong Zou,Gen Liang,Suyun Pu,Jinhui Hu,Lu Chen,Zhongzhi Zhu,Yibiao Li,Yubing Huang
Organic & Biomolecular Chemistry Pub Date : 07/14/2020 00:00:00 , DOI:10.1039/D0OB01163K
Abstract

A novel electrochemical synthesis protocol has been achieved for reductive amination between aldehydes and amines in undivided cells at room temperature. Under metal-free and external-reductant-free electrolysis conditions, various important secondary amine products are obtained in moderate-to-high yields. Deuterium-labeling experiments have demonstrated that low-toxicity DMSO acts both as a solvent and a H-donor in the reaction. On this basis, various deuterium-labeled products with good-to-excellent D-incorporation have been synthesized by using DMSO-d6 as a solvent. Furthermore, a molecule with GR-antagonistic activity has been synthesized through further sulfonylation.

Graphical abstract: Direct electrochemical reductive amination between aldehydes and amines with a H/D-donor solvent
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