Key Laboratory of Organofluorine Chemistry and Collaborative Innovation Center of Chemistry for Life Sciences, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences , 345 Lingling Road, Shanghai 200032, China.
School of Materials and Chemical Engineering, Ningbo University of Technology , No. 201 Fenghua Road, Ningbo 315211, China.
J Am Chem Soc. 2017 Sep 13;139(36):12430-12433. doi: 10.1021/jacs.7b07944. Epub 2017 Aug 30.
The silver-catalyzed decarboxylative trifluoromethylation of aliphatic carboxylic acids is described. With AgNO as the catalyst and KSO as the oxidant, the reactions of aliphatic carboxylic acids with (bpy)Cu(CF) (bpy = 2,2'-bipyridine) and ZnMe in aqueous acetonitrile at 40 °C afford the corresponding decarboxylative trifluoromethylation products in good yield. The protocol is applicable to various primary and secondary alkyl carboxylic acids and exhibits wide functional group compatibility. Mechanistic studies reveal the intermediacy of Cu(CF)Me, which undergoes reductive elimination and subsequent oxidation to give Cu(CF) as the active species responsible for the trifluoromethylation of alkyl radicals.
描述了银催化的脂肪族羧酸脱羧三氟甲基化反应。以 AgNO3 为催化剂,KSO3 为氧化剂,在 40°C 的水-乙腈中,脂肪族羧酸与 (bpy)Cu(CF3)2 (bpy = 2,2'-联吡啶)和 ZnMe 反应,以良好的收率得到相应的脱羧三氟甲基化产物。该方案适用于各种伯和仲烷基羧酸,并表现出广泛的官能团兼容性。机理研究揭示了 Cu(CF3)Me 的中间体,其经历还原消除,随后氧化生成 Cu(CF3),作为负责烷基自由基三氟甲基化的活性物种。