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Butyl Chloride → 2-(3-Phenoxyphenyl)hexanenitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Butyl Chloride | HCID 8005 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | m-Phenoxybenzyl cyanide | HCID 40075 | — |
| 触媒 | Tetraethylammonium Bromide | HCID 6285 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 2-(3-Phenoxyphenyl)hexanenitrile | HCID 23468933 | 54.8% |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04259339 |
| 出典データセット | uspto-grants-1981_03 |
| ORD ID | ord-6d9cf5bcc342455dbac8b50fec879111 |
| 出典メモ | uspto-grants-1981_03 |