Sun Hong-Bin, Hua Ruimao, Yin Yingwu
Key Laboratory of Organic Optoelectronics & Molecular Engineering of Ministry of Education, Beijing 100084, China.
Molecules. 2006 Apr 10;11(4):263-71. doi: 10.3390/11040263.
Esterifications of carboxylic acids with equimolar amount of alcohols could be efficiently catalyzed by ZrOCl(2) x 8H(2)O. Acrylate esters were obtained in good yields under solvent-free conditions at ambient temperature. The esterification of other carboxylic acids with alcohols also proceeded at ambient temperature or at 50 oC to afford esters in high yields. If the esterification was performed in toluene under azeotropic reflux conditions to remove water, both the catalytic activity of ZrOCl(2) x 8H(2)O and the rate of esterification could be increased greatly. Furthermore, in the present catalytic system, the esters could be easily separated from the reaction mixtures and the catalyst could be easily recovered and reused.
用等摩尔量的醇对羧酸进行酯化反应可被八水合氧氯化锆高效催化。在无溶剂条件下于室温可高产率地得到丙烯酸酯。其他羧酸与醇的酯化反应也能在室温或50℃下进行,以高产率得到酯。如果酯化反应在甲苯中于共沸回流条件下进行以除去水,则八水合氧氯化锆的催化活性和酯化速率都可大大提高。此外,在本催化体系中,酯可很容易地从反应混合物中分离出来,催化剂也可很容易地回收并重复使用。