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Vinyltrichlorosilane → Cl3SiCH2CH2SCH(CH3)C6H5
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Vinyltrichlorosilane | HCID 6413 | — |
| 反応物 | 1-Phenylethanethiol | HCID 141850 | — |
| 触媒 | Azobisisobutyronitrile | HCID 6547 | — |
| 生成物 | Cl3SiCH2CH2SCH(CH3)C6H5 | HCID 54184956 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US03957844 |
| 出典データセット | uspto-grants-1976_05 |
| ORD ID | ord-614b595473be49a4b4ac777924a35266 |
| 出典メモ | uspto-grants-1976_05 |