Palladium Catalyzed Aminocarbonylation of Benzylic Ammonium Triflates with Nitroarenes: Synthesis of Phenylacetamides
作者:Li‐Miao Yang、Shan‐Shan Li、You‐Ya Zhang、Jin‐Liang Lu、Jing‐Tong Deng、Ai‐Jun Ma、Xiang‐Zhi Zhang、Shu‐Yu Zhang、Jin‐Bao Peng
DOI:10.1002/adsc.202001561
日期:2021.4.13
A palladium catalyzed reductive aminocarbonylation of benzylic ammonium triflates with nitroarenes for the synthesis of phenylacetamides was developed. Using Pd(acac)2/DPPF catalyst system, a range of different substituted phenylacetamides were prepared in moderate to good yields from benzylic ammonium triflates and nitroarenes through Csp3−N bond cleavage. A variety of alkyl, aryl, and halide substituents
开发了钯催化的苄基三氟甲磺酸铵与硝基芳烃的还原性氨基羰基化反应,用于合成苯乙酰胺。使用Pd(acac)2 / DPPF催化剂体系,通过Csp 3 -N键裂解,从苄基三氟甲磺酸铵和硝基芳烃以中等到良好的产率制备了一系列不同的取代苯基乙酰胺。可以在两个底物上使用多种烷基,芳基和卤化物取代基,并且可以容许许多有用的官能团。