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HRID 442051作成日:2026年10月27日

Styrene → (2-Phenylethyl)trichlorosilane

https://huagongshe.com/reaction/442051

反応式

関与物質

役割名称HCID仕込み量
反応物StyreneHCID 7501—
反応物SilaneHCID 23953—
反応物TrichlorosilaneHCID 24811—
触媒Chloroplatinic acidHCID 61859—
触媒Phenol, bis(1,1-dimethylethyl)-4-methyl-HCID 3034427—
溶媒EthyleneHCID 6325—
溶媒Dimethyl EtherHCID 8254—
生成物(2-Phenylethyl)trichlorosilaneHCID 7032794.2%

反応条件

温度90 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04044037
出典データセットuspto-grants-1977_08
ORD IDord-00e0f416c9bb42c99dc3dae430b350ce
出典メモuspto-grants-1977_08