Tang Shan, Wang Siyuan, Liu Yichang, Cong Hengjiang, Lei Aiwen
College of Chemistry and Molecular Sciences, Institute for Advanced Studies (IAS), Wuhan University, Wuhan, 430072, Hubei, P. R. China.
State Key Laboratory for Oxo Synthesis and Selective Oxidation, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou, 730000, P. R. China.
Angew Chem Int Ed Engl. 2018 Apr 16;57(17):4737-4741. doi: 10.1002/anie.201800240. Epub 2018 Mar 24.
Dehydrogenative C-H/N-H cross-coupling serves as one of the most straightforward and atom-economical approaches for C-N bond formation. In this work, an electrochemical reaction protocol has been developed for the oxidative C-H amination of unprotected phenols under undivided electrolytic conditions. Neither metal catalysts nor chemical oxidants are needed to facilitate the dehydrogenation process. A series of triarylamine derivatives could be obtained with good functional-group tolerance. The electrolysis is scalable and can be performed at ambient conditions.
脱氢C-H/N-H交叉偶联是形成C-N键最直接且原子经济的方法之一。在这项工作中,已开发出一种电化学反应方案,用于在未分隔的电解条件下对未保护的酚进行氧化C-H胺化反应。促进脱氢过程既不需要金属催化剂也不需要化学氧化剂。可以获得一系列具有良好官能团耐受性的三芳基胺衍生物。该电解反应具有可扩展性,且可在环境条件下进行。