Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Butyl Chloride → 2-(4-Phenylthiophenyl) hexanenitrile
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Butyl Chloride | HCID 8005 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | [4-(Phenylsulfanyl)phenyl]acetonitrile | HCID 238605 | — |
| 촉매 | Tetraethylammonium Bromide | HCID 6285 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 2-(4-Phenylthiophenyl) hexanenitrile | HCID 54422980 | 65.1% |
반응 단계
To a mixture of 41 g (0.18 mole) of 4-phenylthiobenzyl cyanide, 18 g (0.19 mole) of butyl chloride and 2 g of tetraethylammonium bromide is added 16 g (0.2 mole) of 50% sodium hydroxide solution dropwise at room temperature with stirring. The reaction mixture is heated at 85° for 1/2 hour and then an additional 16 g (0.2 mole) of 50% sodium hydroxide solution are added. Heating is continued for another 1/2 hour. The reaction mixture is poured into water and extracted with ether. The combined ether extracts are washed with water, saturated sodium chloride solution and dried over MgSO4. Solvent is evaporated to give 47 g of a crude product. Vacuum distillation (173°-180°/0.05 mm) gives 33 g of pure product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04259339 |
| 출처 데이터셋 | uspto-grants-1981_03 |
| ORD ID | ord-1d8b680913c54b35923d1760dd742b70 |
| 출처 메모 | uspto-grants-1981_03 |