1.3.4. Transesterification reaction of 2-methoxycarbonylethyldichlorotin hydroxide

  • Yingying Xu, Wugai An, Wenchao Ding, Haijian Liu, Laijin Tian*
DOI: https://doi.org/10.21060/cis.v1i3.2014

Abstract

The title compound, CH3OCOCH2CH2SnCl2(OH) (1), readily undergotransesterification into the corresponding analogues, ROCOCH2CH2SnCl2(OH) (R = CH3CH2, 2; CH3CH2CH2, 3; CH2=CHCH2,4), when reacted with an alcohol ROH under reflux. The structural featuresof these compounds have been described, and the possible mechanismof the transesterification reaction has been suggested.

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How to Cite
Ding, Haijian Liu, Laijin Tian*, Y. X. W. A. W. (1). 1.3.4. Transesterification reaction of 2-methoxycarbonylethyldichlorotin hydroxide. Communications in Inorganic Synthesis, 1(3). https://doi.org/10.21060/cis.v1i3.2014
Issue
Vol 1 No 3 (2013)
Section
Artículos