Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Vinyltrichlorosilane → Cl3SiCH2CH2SCH(CH3)C6H5
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Vinyltrichlorosilane | HCID 6413 | — |
| 반응물 | 1-Phenylethanethiol | HCID 141850 | — |
| 촉매 | Azobisisobutyronitrile | HCID 6547 | — |
| 생성물 | Cl3SiCH2CH2SCH(CH3)C6H5 | HCID 54184956 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US03957844 |
| 출처 데이터셋 | uspto-grants-1976_05 |
| ORD ID | ord-614b595473be49a4b4ac777924a35266 |
| 출처 메모 | uspto-grants-1976_05 |