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Triethoxysilane is raw material for synthesis of silane addition agent and silicon oil. It is used as a reducing agent.
Miki Murata; Masanori Ishikura; Masayuki Nagata; Shinji Watanabe; and Yuzuru Masuda. Rhodium(I)-Catalyzed Silylation of Aryl Halides with Triethoxysilane:? Practical Synthetic Route to Aryltriethoxysilanes. Org. Lett. 2002, 4 (11), 1843-1845.
Amy S. Manoso and Philip DeShong. Improved Synthesis of Aryltriethoxysilanes via Palladium(0)-Catalyzed Silylation of Aryl Iodides and Bromides with Triethoxysilane. J. Org. Chem. 2001, 66 (22), 7449-7455.
In the presence of KF or CsF, reduces aldehydes and ketones to alcohols (via the silyl ether): Tetrahedron, 37, 2165 (1981). With CsF, enones can be reduced selectively to allylic alcohols in high yield: Tetrahedron., 39, 999 (1983).
Versatile hydrosilylating agent. For use in combination with Ti(O-i-Pr) 4 in a catalytic system for reduction of esters to alcohols, see: J. Org. Chem ., 57, 3751 (1992). CAUTION! Highly pyrophoric SiH 4 can form in this reaction: J. Org. Chem., 57, 3221 (1993).
The same system effects the otherwise difficult reduction of phosphine oxides to phosphines. The products may be reacted in situ with alkyl halides to give a convenient one-pot conversion of phosphine oxides to phosphonium salts: Tetrahedron Lett., 35, 625 (1994).
Pd(0)-catalyzed silylation of aryl iodides provides a route to aryl triethoxysilanes: J. Org. Chem., 62, 8569 (1997).
Gefahrenhinweise (EU): H226-H330-H314-H318
Flammable liquid and vapour. Fatal if inhaled. Causes severe skin burns and eye damage. Causes serious eye damage.
Obtain special instructions before use. Wear protective gloves and eye/face protection. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.