K2CO3-promoted synthesis of amides from 1-aryl-2,2,2-trifluoroethanones and amines under mild conditions

被引:6
作者
Zhong, Pinyong [1 ]
Wang, Yu-Chao [1 ]
Liu, Jin-Biao [1 ]
Zhang, Linjun [2 ]
Luo, Nianhua [3 ]
机构
[1] Jiangxi Univ Sci & Technol, Jiangxi Prov Key Lab Funct Mol Mat Chem, Ganzhou 341000, Peoples R China
[2] Jiangxi Prov Zhonggantou Survey & Design Co Ltd, Nanchang 330029, Peoples R China
[3] Gannan Med Univ, Sch Pharmaceut Sci, Ganzhou 341000, Peoples R China
基金
中国国家自然科学基金;
关键词
C BOND-CLEAVAGE; ONE-POT; OXIDATIVE AMIDATION; SIMPLE KETONES; HALLER-BAUER; ACID; ALDEHYDES; SOLVENT; ESTERS; CONVERSION;
D O I
10.1039/d3ra03329e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A base-promoted amidation of 1-aryl-2,2,2-trifluoroethanones with amines via Haller-Bauer reaction has been developed. In this reaction, the direct transformation of 1-aryl-2,2,2-trifluoroethanones into amides via C(O)-C bond cleavage occurs without the use of any stoichiometric chemical oxidants or transition-metal catalysts. A series of primary and secondary amines are shown to be compatible with this transformation, and several pharmaceutical molecules were synthesized.
引用
收藏
页码:18160 / 18164
页数:5
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