Hu Jiayin, Ma Jun, Lu Lu, Qian Qingli, Zhang Zhaofu, Xie Chao, Han Buxing
Beijing National Laboratory for Molecular Sciences (BNLMS), CAS Key Laboratory of Colloid and Interface and Thermodynamics Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, P.R. China.
School of Chemistry and Chemical Engineering, University of Chinese Academy of Sciences, Beijing, 100049, P.R. China.
ChemSusChem. 2017 Mar 22;10(6):1292-1297. doi: 10.1002/cssc.201601773. Epub 2017 Feb 7.
Synthesis of asymmetrical organic carbonates from the renewable and inexpensive CO 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 CO , 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.
由可再生且廉价的一氧化碳合成不对称有机碳酸酯具有重要意义,但也具有挑战性,尤其是在环境条件下。在此,我们发现一些金属盐/离子液体催化剂体系对由一氧化碳、炔丙醇和伯醇合成不对称有机碳酸酯具有高活性。特别是,氯化银/1-丁基-3-甲基咪唑醋酸盐([Bmim][OAc])体系在室温及大气压下对多种底物的反应非常有效,不对称有机碳酸酯的产率可接近100%。该催化剂体系可至少重复使用五次而不改变其催化性能,并且能够容易地回收再利用。详细研究表明,氯化银和[Bmim][OAc]协同催化反应,从而产生独特的催化性能。