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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892626Generated: November 2, 2026

Methanol → methoxytributyl silane

https://huagongshe.com/reaction/1892626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTrichlorosilaneHCID 24811—
ReactantTributylsilaneHCID 269923—
ReactantHCID 178418265HCID 178418265—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventWaterHCID 962—
Productmethoxytributyl silaneHCID 576156—

Reaction Steps

In a 500 ml four-neck flask provided with reflux condenser, precision glass stirrer and thermometer, 1.2 g of 5% palladium on activated carbon, water-free (commercially available from Sigma-Aldrich Corp., USA) were suspended in 23.7 g of methanol. 124 g of tri-n-butylsilane (prepared from trichlorosilane and n-butylmagnesium chloride by a method customary in organic chemistry) were subsequently introduced at room temperature over a period of one hour while stirring. After addition of the first drops of the SiH-functional siloxane, spontaneous hydrogen evolution commenced. The temperature of the reaction mixture rose to a maximum of 35° C. After the addition was complete, the mixture was allowed to react further until gas evolution could no longer be observed at the attached bubble counter, the black precipitate was filtered on a pressure filter and the colorless clear filtrate was distilled via a 20 cm Vigreux column. After the first fraction, which according to gas-chromatographic analysis consisted mainly of methanol, 134 g of tributylmethoxysilane having a GC purity of 99.5% by area distilled over at a boiling temperature of 112° C. at 10 hPa.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507709B2
Source datasetuspto-grants-2013_08
ORD IDord-045988ef579f4a7793979694819e46bd
Source noteuspto-grants-2013_08