6421-39-2Relevant academic research and scientific papers
Versatile method for introduction of bulky substituents to alkoxychlorosilanes
Masaoka, Shin,Banno, Tadashi,Ishikawa, Mitsuo
, p. 182 - 192 (2007/10/03)
The reactions of various alkoxytrichlorosilanes prepared in situ from tetrachlorosilane and alcohols, with Grignard reagents bearing a bulky substituent such as the isopropyl, sec-butyl, and cyclohexyl group afforded triisopropyl-, tri(sec-butyl)-, and tricyclohexylalkoxysilane in high yields. The reactions of n-butoxytrichlorosilane with these Grignard reagents produced triisopropyl-, tri(sec-butyl)-, and tricyclohexyl(n-butoxy)silane in 94%, 96%, and 92% yields, respectively. Methoxymethyldichlorosilane reacted with the same Grignard reagents to give diisopropyl-, di(sec-butyl)-, and dicyclohexylmethoxymethylsilane in 84%, 83%, and 83% yields. Treatment of methoxydimethylchlorosilane with the Grignard reagents readily afforded isopropyl-, sec-butyl-, and cyclohexylmethoxydimethylsilane in excellent yields. Similar treatment of methoxydimethylchlorosilane with tert-butylmagnesium chloride gave tert-butylmethoxydimethylsilane in 62% yield.
Exchange reactions in alkoxy derivatives of silicon and germanium
Chernyshev,Belyakova,Knyazev,Turkel'Taub',Ovsyankina,Ugarova,Yakovleva
, p. 650 - 652 (2007/10/03)
Reaction SiCl4+ Ge(OR)4 → GeCl4+ Si(OR)4 was carried out for the first time. Triethoxysilane reduces tetraethoxygermane via intermediate formation of unstable GeH(OEt)3 that transforms into GeO·Et2O or Ge(OH)2.
Reaction of Tetraalkoxysilanes with Alkyl(aryl)chlorosilanes
Chernyshev, E. A.,Komalenkova, N. G.,Tagachenkov, A. A.,Bykovchenko, V. G.
, p. 241 - 243 (2007/10/03)
Alkyl(aryl)trichloro- or dialkyl(diaryl)dichlorosilanes react with tetraalkoxysilanes Si(OMe)4, Si(OEt)4, and Si(OBu)4 to give partially etherfied alkyl(aryl)chlorosilanes RSiCl2(OAlk), RSiCl(OAlk)2, and R2SiCl(OAlk).
