Chinese Journal of Catalysis ›› 2006, Vol. 27 ›› Issue (3): 197-199.

• Articles • Previous Articles     Next Articles

Synthesis of α-Hydroxy Esters by Glyoxylate-Ene Reaction in Lewis Acid Chloroaluminate Ionic Liquids

SHEN Zhenlu*, HE Xijun, MO Weimin, XIE Yi, HU Baoxiang, SUN Nan   

  1. College of Chemical Engineering and Material Science, Zhejiang University of Technology, Hangzhou 310032, Zhejiang, China
  • Received:2006-03-25 Online:2006-03-25 Published:1984-10-26

Abstract: The chloroaluminate ionic liquid, composed of AlCl3 and 1-butyl-3-methylimidazolium chloride ([bmim]Cl), is used as the solvent and catalyst to synthesize α-hydroxy esters from alkene and glyoxylate via the glyoxylate-ene reaction. Under the reaction conditions of 15 ℃, 4 h, and AlCl3/[bmim]Cl molar ratio of 2, the ethyl α-hydroxy-4-phenyl-4-pentenoate with high yield (95.2%) is obtained in the reaction of α-methyl styrene and ethyl glyoxylate. Other α-hydroxy esters can also be obtained in high yields through the glyoxylate-ene reaction. Moreover, the chloroaluminate ionic liquid can be reused several times.

Key words: glyoxylate-ene reaction, ionic liquid, α-hydroxy ester, aluminium chloride, glyoxylate