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Synthesis of Primary and Secondary Amines via Electrochemical Reduction of Hydrazines
Organic Letters ( IF 4.9 ) Pub Date : 2024-12-13 , DOI: 10.1021/acs.orglett.4c04040
Dong Wang, Qiulu Wang, Mingxia Liu, Zihan Liu, Zixuan Wang, Wenhui Ji, Yu Wang, Jin Wang

We herein introduce an electrochemical route for the N–N bond cleavage of hydrazines. This mild and green methodology utilized readily available mono- and 1,1-disubstituted hydrazines or their HCl salts as starting materials to access a broad scope of primary and secondary amines in high yields. The mechanistic investigation suggests that the amine product is formed by consecutive SET reduction, and utilization of a hydrazine HCl salt is important for providing sufficient conductivity and acidity to facilitate this reaction.

中文翻译:


通过肼的电化学还原合成伯胺和仲胺



我们在这里介绍了一种用于肼 N-N 键裂解的电化学路线。这种温和、绿色的方法利用现成的单取代和 1,1-二取代肼或其 HCl 盐作为起始材料,以高产率获得广泛的伯胺和仲胺。机理研究表明,胺产物是由连续的 SET 还原形成的,利用盐酸肼对于提供足够的电导率和酸度以促进该反应非常重要。
更新日期:2024-12-13
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