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Updated: May 11, 2026

Efficient Synthesis of All-Carbon Quaternary Centers via the Conjugate Addition of Functionalized Monoorganozinc Bromides
Published on: May 26, 2019
Silica-anchored organotin trichloride: a recyclable and clean organotin catalyst for transesterification reactions
Thierry Toupance1, Laetitia Renard, Bernard Jousseaume
1University of Bordeaux, Institut des Sciences Moléculaires, ISM UMR 5255 CNRS, C2M group, 33405 Talence Cédex, France. t.toupance@ism.u-bordeaux1.fr
Abstract:
A new synthetic scheme towards silica-supported organotrichlorotin derivatives has been developed. It involves the synthesis of (11-triethoxysilyl)undecyltricyclohexyltin, followed by sol-gel processing and, subsequently in the formation of the resulting hybrid silica, by electrophilic substitution of the tricyclohexyltin function by the target grafted trichlorotin using tin tetrachloride. HR-MAS (119)Sn and CP-MAS (29)Si NMR combined with N2-sorption and TEM measurements evidenced the formation of a mesoporous organic-inorganic hybrid silica including a functionally pure supported-organotrichlorotin species. This silica-grafted organotrichlorotin displays a satisfactory catalytic activity in the transesterification of ethyl acetate by 1-octanol. The catalyst could be recycled four times without significant loss of activity. Furthermore, tin leaching below 10 ppm evidences the benefits of the proposed strategy to limit tin contamination of the final products.
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