Electrochemically catalyzed synthesis of cyclic carbonates from CO2 and propargyl alcohols

被引:28
|
作者
Yuan, Gao-Qing [1 ]
Zhu, Guo-Jun [1 ]
Chang, Xiao-Ying [1 ]
Qi, Chao-Rong [1 ]
Jiang, Huan-Feng [1 ]
机构
[1] S China Univ Technol, Sch Chem & Chem Engn, Guangzhou 510640, Peoples R China
基金
中国国家自然科学基金;
关键词
N BOND FORMATION; IONIC LIQUID; AROMATIC KETONES; ELECTROCATALYTIC CARBOXYLATION; 6-AMINONICOTINIC ACID; SUBSTITUTED ALKENES; RING CARBOXYLATION; ACTIVATED OLEFINS; CYANOACETIC ACID; SILVER CATHODES;
D O I
10.1016/j.tet.2010.10.039
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A convenient and efficient electrochemical method has been developed for the synthesis of the alpha-alkylidene cyclic carbonates from carbon dioxide (CO2) and propargyl alcohols at room temperature. The electrosynthesis was successfully carried out with a copper anode and a nickel cathode in an undivided cell containing n-Bu4NBr-MeCN electrolyte with a constant current under 3 MPa pressure of CO2, and the a-alkylidene cyclic carbonates were obtained in good to excellent isolated yields in the secondary and tertiary terminal propargylic alcohols cases. The experimental results show that the electrogenerated Cu+ ions and strong bases in situ could efficiently catalyze or promote the coupling reaction under the cooperation of electrolytic medium MeCN and supporting electrolyte n-Bu4NBr. The plausible mechanism of the coupling reaction was also discussed briefly. (c) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:9981 / 9985
页数:5
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