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4-Chlorobutyronitrile → 4-(7-bromo-1H-indol-3-yl)butanenitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Chlorobutyronitrile | HCID 12336 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | 7-Bromoindole | HCID 2757020 | — |
| 反応物 | HCID 178418443 | HCID 178418443 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 4-(7-bromo-1H-indol-3-yl)butanenitrile | HCID 68693387 | — |
反応手順
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).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07728023B2 |
| 出典データセット | uspto-grants-2010_06 |
| ORD ID | ord-27fdefc4bc05481e8d695825b2e4ecdb |
| 出典メモ | uspto-grants-2010_06 |