Chem. J. Chinese Universities ›› 2000, Vol. 21 ›› Issue (5): 740.

• Articles • Previous Articles     Next Articles

Studies on the Reaction of 1,2,3-Trisubstituted Electron-deficient Cyclopropane Derivatives with Methanol

CAO Wei-Guo1,2, DING Wei-Yu1, TONG Wei-Qi1, LIU Xin1, QIU Meng-Yao1   

  1. 1. Department of Chemistry, Shanghai University, Shanghai 201800, China;
    2. State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, China
  • Received:1999-04-12 Online:2000-05-24 Published:2000-05-24

Abstract: In this paper, the reaction of 1, 2, 3-trisubstituted electron-deficient cyclopropane derivatives ets-1-benzoyl-2-p-substituted phenyl-6, 6-dimethyl-5, 7-dioxo-spiro-[2,5]-4, 8-octadiones with methanol was studied. The structures of the reaction products were confirmed as methyl β-benzoyl-γ-methoxy-γ-p- substituted phenylbutyrates by means of IR, MS, microanalysis, 1H, 13C NMRspectroscopies and APTtechniques. The reaction mechanism for the formation of the product was also proposed.

Key words: 1, 2, 3-Trisubstituted cyclopropane, Methanolysis, Methyl butyrate

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