Wu Ya-Nan, Fu Ming-Chen, Shang Rui, Fu Yao
Hefei National Laboratory for Physical Sciences at the Microscale, CAS Key Laboratory of Urban Pollutant Conversion, Anhui Province Key Laboratory of Biomass Clean Energy, iChEM, University of Science and Technology of China, Hefei 230026, China.
Chem Commun (Camb). 2020 Apr 9;56(29):4067-4069. doi: 10.1039/d0cc01363c.
A protocol for the Ni-catalyzed carboxylation of aryl iodides with formate has been developed with good functional group compatibility for the synthesis of a variety of aromatic carboxylic acids under mild conditions. The reaction tolerates other functionalities for cross-coupling, such as aryl bromide, aryl chloride, aryl tosylate, and aryl pinacol boronate. The reaction proceeds through a carbonylation process with in situ generated carbon monoxide in the presence of a catalytic amount of acetic anhydride and lithium formate, avoiding the use of gaseous CO. The strategy of CO recycling in catalytic amounts is critical for the success of the reaction.
已开发出一种用于镍催化芳基碘化物与甲酸盐进行羧化反应的方案,该方案在温和条件下合成多种芳香羧酸时具有良好的官能团兼容性。该反应能耐受用于交叉偶联的其他官能团,如芳基溴化物、芳基氯化物、芳基甲苯磺酸盐和芳基频哪醇硼酸酯。反应在催化量的乙酸酐和甲酸锂存在下通过原位生成一氧化碳的羰基化过程进行,避免了使用气态一氧化碳。催化量的一氧化碳循环利用策略对反应的成功至关重要。