| Literature DB >> 28070981 |
Jiayin Hu1,2, Jun Ma1, Lu Lu1,2, Qingli Qian1, Zhaofu Zhang1, Chao Xie1,2, Buxing Han1,2.
Abstract
Synthesis of asymmetrical organic carbonates from the renewable and inexpensive CO2 is of great importance but also challenging, especially at ambient conditions. Herein, we found that some metal salt/ionic liquid catalyst systems were highly active for the synthesis of asymmetrical organic carbonates from CO2 , propargylic alcohols, and primary alcohols. Especially, the AgCl/1-butyl-3-methylimidazolium acetate ([Bmim][OAc]) system was very efficient for the reactions of a wide range of substrates at room temperature and atmospheric pressure, and the yields of the asymmetrical organic carbonates could approach 100 %. The catalyst system could be reused at least five times without changing its catalytic performance, and could be easily recovered and reused. A detailed study indicated that AgCl and [Bmim][OAc] catalyzed the reactions cooperatively, resulting in unique catalytic performance.Entities:
Keywords: asymmetrical carbonates; carbon dioxide; fixation; ionic liquids; propargylic alcohols
Mesh:
Substances:
Year: 2017 PMID: 28070981 DOI: 10.1002/cssc.201601773
Source DB: PubMed Journal: ChemSusChem ISSN: 1864-5631 Impact factor: 8.928