Synthesis of α-CF3 Amides via Palladium-Catalyzed Carbonylation of 2-Bromo-3,3,3-trifluoropropene

被引:6
作者
Wen, Xiao Rui [1 ]
Zhu, Wen Qing [1 ]
Zhang, Cai Lin [1 ]
Li, Hong [1 ]
Zhang, Jin [1 ]
Yang, Min Ge [1 ]
Kou, Yong Li [2 ]
Liu, Yu Xia [3 ]
Li, Yang [1 ]
机构
[1] Xian Polytech Univ, Sch Environm & Chem Engn, Xian 710048, Peoples R China
[2] Shaanxi Coal Chem Ind Technol Res Inst Co Ltd, Xian 710065, Peoples R China
[3] Northwest Univ, Coll Food Sci & Technol, Shaanxi Nat Carbohydrate Resource Engn Res Ctr, Xian 710127, Peoples R China
来源
ACS OMEGA | 2023年
基金
中国国家自然科学基金;
关键词
MANNICH-TYPE REACTION; BETA-LACTAMS; ASYMMETRIC FLUORINATION; AMINO-ACIDS; C(SP(3))-H; TRIFLUOROMETHYLATION; CYCLOADDITION; AMIDATION; ALKENES;
D O I
10.1021/acsomega.2c08206
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Amide compounds are important organic com-pounds, which play an important role in biomedical chemistry, materials science, life science, and other fields. The synthesis of alpha- CF3 amides, especially compounds containing 3-(trifluoromethyl)-1,3,4,5-tetrahydro-2H-benzo[b][1,4]diazepine-2-one, has long been a challenge due to the tensile properties and instability of the rings. Here, we report an example of palladium-catalyzed carbonylation of CF3-containing olefin to form alpha-CF3 acrylamide. By controlling the ligands, we can get different amide compounds as products. This method has good substrate adaptability and functional group tolerance.
引用
收藏
页码:7128 / 7134
页数:7
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