Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
4-Chlorobutyronitrile → 4-(7-bromo-1H-indol-3-yl)butanenitrile
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 4-Chlorobutyronitrile | HCID 12336 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | 7-Bromoindole | HCID 2757020 | — |
| 반응물 | HCID 178418443 | HCID 178418443 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 4-(7-bromo-1H-indol-3-yl)butanenitrile | HCID 68693387 | — |
반응 단계
To an anhydrous toluene (12 mL) solution of 7-bromoindole (1.0 g) and 4-chlorobutyronitrile (0.26 g), ethylmagnesium bromide (3.0M diethyl ether solution; 1.7 mL) was added dropwise under ice cooling and the mixture was heated to reflux for 4.5 hours. To the reaction mixture, an aqueous saturated ammonium chloride solution was added under ice cooling, followed by extraction with ethyl acetate. The organic layer was washed in turn with water and saturated saline, dried over anhydrous magnesium sulfate and then concentrated. The residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=90:10→70:30) to obtain the titled compound having the following physical properties (0.40 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07728023B2 |
| 출처 데이터셋 | uspto-grants-2010_06 |
| ORD ID | ord-27fdefc4bc05481e8d695825b2e4ecdb |
| 출처 메모 | uspto-grants-2010_06 |