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Selective Formation of Alkoxychlorosilanes and Organotrialkoxysilane with Four Different Substituents by Intermolecular Exchange Reaction
Authors:Yasuhiro Tamura  Prof. Hiroaki Wada  Prof. Atsushi Shimojima  Prof. Kazuyuki Kuroda
Affiliation:1. Department of Applied Chemistry, Faculty of Science and Engineering, Waseda University, Tokyo, Japan;2. Kagami Memorial Research Institute for Materials Science and Technology, Waseda University, Tokyo, Japan
Abstract:Alkoxychlorosilanes are scientifically and industrially important toward preparing silicone and silica as well as preparation of siloxane‐based nanomaterials by stepwise reactions of Si?OR (R=alkyl) and Si?Cl groups. Intermolecular exchange of alkoxy and chloro groups between alkoxysilanes and chlorosilanes (functional group exchange reaction) provides an efficient and environmentally benign route to alkoxychlorosilanes. BiCl3 as a Lewis acid catalyst can promote the functional group exchange reactions more efficiently than conventional acid catalysts. Higher reactivity has been observed for chlorosilanes with smaller numbers of Si?CH3 groups and for alkoxysilanes with larger numbers of Si?CH3 groups. The reaction mechanism is proposed and selective syntheses of alkoxychlorosilanes are demonstrated. These findings also enable us to synthesize an organotrialkoxysilane with four different substituents.
Keywords:alkoxysilane  chlorosilane  exchange reaction  Lewis acid  selective synthesis
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