Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Butyl Chloride → 2-(3-Phenoxyphenyl)hexanenitrile
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Butyl Chloride | HCID 8005 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | m-Phenoxybenzyl cyanide | HCID 40075 | — |
| 촉매 | Tetraethylammonium Bromide | HCID 6285 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 2-(3-Phenoxyphenyl)hexanenitrile | HCID 23468933 | 54.8% |
반응 단계
Into a three-necked 500 ml round-bottom flask are charged 35 g (0.17 mole) of m-phenoxybenzyl cyanide, 16.3 g (0.17 mole) of butyl chloride 4 g of tetraethylammonium bromide. To this mixture is added 27 g (0.34 mole) of 50% sodium hydroxide solution dropwise with stirring. The reaction mixture is heated at 90° for three hours. It is then poured into water and extracted with hexane. The combined hexane extracts are washed with water and dried over MgSO4. Solvent is evaporated to give 39 g of crude product. Vacuum distillation (149°-155°/0.2 mm) provides 24.7 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-6d9cf5bcc342455dbac8b50fec879111 |
| 출처 메모 | uspto-grants-1981_03 |