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通过电化学还原实现三烷基膦与芳基卤化物的无催化剂磷酸化反应。

Catalyst-free phosphorylation of aryl halides with trialkyl phosphites through electrochemical reduction.

机构信息

Beijing National Laboratory of Molecular Sciences (BNLMS), Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry, Peking University, Beijing 100871, China.

出版信息

Chem Commun (Camb). 2019 Nov 19;55(93):14035-14038. doi: 10.1039/c9cc07069a.

Abstract

A catalyst-free electrochemical cross-coupling reaction of aryl halides with trialkyl phosphite has been developed. This reaction proceeds in an undivided cell with a low-cost Ni anode and a graphite cathode under mild and neutral conditions. A wide range of functional groups are well-tolerated and the phosphorylated product can be obtained on the gram scale, showing that this transformation has the potential to be a valuable method for the construction of aromatic carbon-phosphorus bonds.

摘要

发展了一种无需催化剂的芳基卤化物与三烷基膦的电化学交叉偶联反应。该反应在一个低成本的 Ni 阳极和石墨阴极的无分隔电池中,在温和、中性条件下进行。该反应具有广泛的官能团耐受性,并且可以克级规模地获得磷酸化产物,表明该转化有可能成为构建芳基碳-磷键的一种有价值的方法。

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