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Ethyl Bromide → 4-Chloro-4'-ethylthiomethylbenzophenone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethyl Bromide | HCID 6332 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | 4-Chloro-4'-mercaptomethylbenzophenone | HCID 19689380 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 4-Chloro-4'-ethylthiomethylbenzophenone | HCID 19689354 | 79.1% |
反応手順
4-chloro-4'-mercaptomethylbenzophenone (16.0 g), ethyl bromide (7.4 g) and potassium hydroxide (4.3 g) were added to methanol (250 ml), and the mixture was stirred for 30 minutes under reflux. The reaction mixture was cooled to room temperature and then concentrated. Water was added to the residue, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with water and then dried over anhydrous magnesium sulfate and concentrated. The residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=10:1) to obtain the desired product 14.0 g, melting point: 33° to 34° C., yield: 79%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05728699 |
| 出典データセット | uspto-grants-1998_03 |
| ORD ID | ord-854622046616431a8dec648c46bb4905 |
| 出典メモ | uspto-grants-1998_03 |