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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442051Generated: October 26, 2026

Styrene → (2-Phenylethyl)trichlorosilane

https://huagongshe.com/reaction/442051

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStyreneHCID 7501—
ReactantSilaneHCID 23953—
ReactantTrichlorosilaneHCID 24811—
CatalystChloroplatinic acidHCID 61859—
CatalystPhenol, bis(1,1-dimethylethyl)-4-methyl-HCID 3034427—
SolventEthyleneHCID 6325—
SolventDimethyl EtherHCID 8254—
Product(2-Phenylethyl)trichlorosilaneHCID 7032794.2%

Reaction Conditions

Temperature90 °C

Reaction Steps

About 468 grams (4.5 moles) of styrene and about 0.5 grams of di-t-butyl-p-cresol were charged to a one liter, three necked round bottom flask fitted with a magnetic stirrer, thermometer, dropping funnel and reflux condenser bearing a nitrogen by-pass on the vent. While stirring the flask contents were heated to 90° C, and a sufficient amount of about a 2% solution of chloroplatinic acid catalyst dissolved in dimethylether of ethylene glycok to give about 25 parts by weight of plantinum per million parts by weight of reactants was added. Then about 610 grams (4.5 moles) of trichlorosilane were slowly and continuously added via the dropping funnel over a one and one-half hour period while maintaining the reaction temperature at 90°-95° C. A vapor phase chromatogram on the reaction contents indicated there was an essentially complete conversion to product. The crude silane reaction product was then refined by a one plate distillation at 0.1 mm. pressure to yield about 1015 grams (4.24 moles) of phenylethyltrichlorosilane product ##STR22## (94.5% conversion) which had a boiling point of about 63°-64° C./0.1 mm Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04044037
Source datasetuspto-grants-1977_08
ORD IDord-00e0f416c9bb42c99dc3dae430b350ce
Source noteuspto-grants-1977_08