Liu Chenwei, An Tongshun, Yuan Weiheng, Dai Huiying, Liang Xiaolan, Yin Zhiping
School of Pharmacy, Jiangsu University, Zhenjiang 212013, P. R. China.
Chem Commun (Camb). 2023 Oct 26;59(86):12891-12894. doi: 10.1039/d3cc04126c.
The direct carbonylation of readily available nitro compounds is more attractive and straightforward than the use of traditional amines as nucleophiles. Herein, a practical palladium-catalysed double carbonylation of nitroarenes with -dihaloarenes has been developed for the construction of various -aryl phthalimides. Key to the success of this transformation is the use of Mo(CO), which acts as both a reducing agent and a solid carbonyl source. A wide range of nitroarenes and -dihaloarenes as well as -iodobenzoic acids reacted smoothly to give phthalimides in 27-94% yields.
与使用传统胺作为亲核试剂相比,将易于获得的硝基化合物直接羰基化更具吸引力且更直接。在此,已开发出一种实用的钯催化硝基芳烃与二卤代芳烃的双羰基化反应,用于构建各种芳基邻苯二甲酰亚胺。该转化成功的关键是使用Mo(CO)₆,它既是还原剂又是固体羰基源。多种硝基芳烃、二卤代芳烃以及碘代苯甲酸顺利反应,以27% - 94%的产率得到邻苯二甲酰亚胺。