1.3.4. Transesterification reaction of 2-methoxycarbonylethyldichlorotin hydroxide

Autores/as

  • Yingying Xu, Wugai An, Wenchao Ding, Haijian Liu, Laijin Tian*

DOI:

https://doi.org/10.21060/cis.v1i3.2014

Resumen

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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Número

Vol. 1 Núm. 3 (2013)

Sección

Artículos

Cómo citar

1.3.4. Transesterification reaction of 2-methoxycarbonylethyldichlorotin hydroxide. (2015). Communications in Inorganic Synthesis, 1(3). https://doi.org/10.21060/cis.v1i3.2014