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Triethylamine → alpha-Pivaloyl-alpha-[4-(3-hydroxypropyl)pyrazolyl]-2-chloroacetanilide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 3-(1H-pyrazol-4-yl)propan-1-ol | HCID 3578384 | — |
| 反応物 | alpha-Bromo-2-pivaloyl-2-chloroacetanilide | HCID 19875675 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | alpha-Pivaloyl-alpha-[4-(3-hydroxypropyl)pyrazolyl]-2-chloroacetanilide | HCID 178447087 | 87.4% |
反応手順
56.7 g of 4-(3-hydroxypropyl)pyrazole and 45.5 g of triethylamine were dissolved in 500 ml of chloroform and, under cooling with ice, a solution of 88.8 g of α-bromo-2-pivaloyl-2-chloroacetanilide in 300 ml of chloroform was dropwise added thereto in about 1 hour. After completion of the dropwise addition, the solution was stirred for 2 hours, and the reaction solution was washed twice with 300 ml of dilute hydrochloric acid, then twice with 500 ml of water. The reaction solution was dried with anhydrous sodium sulfate, concentrated, and purified by silica gel chromatography to obtain 88.2 g of oily α-pivaloyl-α-[4-(3-hydroxypropyl)pyrazolyl]-2-chloroacetanilide. (Yield: 78%)
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05151356 |
| 出典データセット | uspto-grants-1992_09 |
| ORD ID | ord-610ee9c4254941dbac0af0a4b1cf4cb2 |
| 出典メモ | uspto-grants-1992_09 |