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Preparation and reactions of some sterically hindered silanols, including [tris(trimethylsilyl)methyl]silanetriol
Authors:Ramadan I Damja  Colin Eaborn
Institution:

School of Chemistry and Molecular Sciences, University of Sussex, Brighton BN1 9QJ Great Britain

Abstract:The silanol TsiSiMe2OH (Tsi = (Me3Si)3C) has been made by hydrolysis of the iodide TsiSiMe2I in H2O/dioxane or H2O/Me2SO. It has been shown to react with some acid chlorides RCOCl (R=Me, Et, CICH2 Ph, 4-O2NC6H4, and 3,5- (O2N)2C6H3) and anhydrides (RCO)2O (R = Me, CF3, or Ph) to give the carboxylates TsiSiMe2OCOR, and with SO2Cl2 to give TsiSiMe2OSO2Cl. The triol TsiSi(OH)3 has been made by treatment of TsiSiH(OH)I with H2O/Me2SO at 150°C or with a mixture of aqueous AgClO4 and an organic solvent. The triol has been shown to react with RCOCl (R = Me, Et, or Ph) or (RCO)2O (R = Ph) to give the corresponding TsiSi(OCOR)3, with (CF3CO)2O to give TsiSi(OH)2(OCOCF3), and with a mixture of Me3SiCl and AgClO4 in benzene or one of Me3Sil and (Me3Si)NH to give TsiSi(OSiMe3)3. The triol is unusually stable, but decomposes at its m.p. of 285–290°C.
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