Ag(I)/(C2H5)4NCl Cooperation Catalysis for Fixing CO2 or Its Derivatives into β-Oxopropylcarbamates

被引:12
|
作者
Zhao, Qing-Ning [1 ]
Song, Qing-Wen [2 ]
Liu, Ping [2 ]
Zhang, Kan [2 ]
Hao, Jian [1 ]
机构
[1] Shanghai Univ, Dept Chem, Shanghai 200444, Peoples R China
[2] Chinese Acad Sci, State Key Lab Coal Convers, Inst Coal Chem, Taiyuan 030001, Shanxi, Peoples R China
来源
CHEMISTRYSELECT | 2018年 / 3卷 / 24期
基金
中国国家自然科学基金;
关键词
Carbon dioxide fixation; Homogeneous catalysis; beta-Oxopropylcarbamates; Silver catalysis; Synthetic method; CARBON-DIOXIDE INCORPORATION; ECO-FRIENDLY PROCESS; PROPARGYLIC ALCOHOLS; CYCLIC CARBONATES; EFFICIENT; TRANSFORMATION; COPPER; ACTIVATION; CONVERSION; MECHANISM;
D O I
10.1002/slct.201801422
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
It remains a great challenge to convert CO2 into high value-added products under ambient pressure. Herein, an efficient dual-component catalytic system, i.e., Ag(I)/(C2H5)(4)NCl was developed for the synthesis of various beta-oxopropylcarbamates via one-pot three-component coupling of CO2, secondary amines and propargylic alcohols under atmospheric pressure. Besides, the strategy avoided the use of any additional ligand and basic species, and excellent selectivity was achieved with a yield of up to 98%. Additionally, C-13(carbonyl)-labeled and control experiments were carefully performed to demonstrate the mechanism. Notably, this new method was also applied efficiently in quantitative chemical fixation of CO2, i.e., the two-component reaction of propargylic alcohols and ammonium carbamates.
引用
收藏
页码:6897 / 6901
页数:5
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