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HRID 1906292作成日:2026年10月27日

Dichlorodiphenylsilane → Dioctadecyldiphenylsilane

https://huagongshe.com/reaction/1906292

反応式

関与物質

役割名称HCID仕込み量
反応物DichlorodiphenylsilaneHCID 6627—
反応物HCID 178442890HCID 178442890—
生成物DioctadecyldiphenylsilaneHCID 435176978%

反応手順

The first portion of the octadecylmagnesium bromide was cooled to 0° and cuprous cyanide (0.12 g 1.34 mmoles) was added with stirring. Then dichlorodiphenylsilane (1.95 ml, 9.27 mmoles) was added. The reaction mixture was stirred at 10° for 140 minutes. Gas chromatographic analysis showed that most of the dichlorodiphenylsilane had disappeared during the first hour of reaction. The mixture was then stirred at room temperature for about 16 hours (i.e. overnight). The reaction mixture was then filtered, quenched with water, and acidified slightly with HCl. After extraction with diethylether, drying (with MgSO4) and removal of solvent, a solid was obtained. Extraction with hot heptane and crystallization provided 4.96 g of dioctadecyldiphenylsilane. The yield was about 78%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04650891
出典データセットuspto-grants-1987_03
ORD IDord-965c22f5de6a4bfa9e31a0a5b952a12b
出典メモuspto-grants-1987_03