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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1076730Generated: October 26, 2026

Vinyltrichlorosilane → HCID 54184956, compound

https://huagongshe.com/reaction/1076730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantVinyltrichlorosilaneHCID 6413—
Reactant1-PhenylethanethiolHCID 141850—
CatalystAzobisisobutyronitrileHCID 6547—
ProductHCID 54184956HCID 54184956—

Reaction Steps

Into a 500 ml. three-necked flask were charged 108 g. (0.78 mole) 1-phenyl-ethanethiol, 126 g. (0.78 mole) vinyltrichlorosilane and 1.2 g. (0.5 weight percent) azobisisobutyronitrile catalyst. The contents were heated and stirred for 6 hours at 80°-90°C. Fractional distillation of the reaction mixture gave the product fraction, Cl3SiCH2CH2SCH(CH3)C6H5, b.p. 110°/0.53 mm Hg. Vapor phase chromatographic analysis of the distilled product (120 g.) showed it contained a mixture of alpha and beta isomers. Yield of (1-phenylethylthio)ethyltrichlorosilane was 85 percent, based on ViSiCl3 reacted.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03957844
Source datasetuspto-grants-1976_05
ORD IDord-614b595473be49a4b4ac777924a35266
Source noteuspto-grants-1976_05