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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 442051Erstellt: 26. Oktober 2026

Styrene → (2-Phenylethyl)trichlorosilane

https://huagongshe.com/reaction/442051

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktStyreneHCID 7501—
EduktSilaneHCID 23953—
EduktTrichlorosilaneHCID 24811—
KatalysatorChloroplatinic acidHCID 61859—
KatalysatorPhenol, bis(1,1-dimethylethyl)-4-methyl-HCID 3034427—
LösungsmittelEthyleneHCID 6325—
LösungsmittelDimethyl EtherHCID 8254—
Produkt(2-Phenylethyl)trichlorosilaneHCID 7032794,2%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04044037
Quelldatensatzuspto-grants-1977_08
ORD IDord-00e0f416c9bb42c99dc3dae430b350ce
Quellennotizuspto-grants-1977_08