関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Acetone Cyanohydrin | HCID 6406 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Dimedone | HCID 31358 | — |
| 反応物 | 4-(Methanesulfonyl)-2-nitrobenzoyl chloride | HCID 14800186 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2-(4-Methylsulphonyl-2-nitrobenzoyl)-5,5-dimethylcyclohexane-1,3-dione | HCID 19937139 | 48.8% |
反応手順
A solution of 4-methylsulphonyl-2-nitrobenzoyl chloride (9.62 g) in dry dichloromethane (50 ml) was added to a stirred solution of triethylamine (5.6 ml) and 5,5-dimethylcyclohexane-1,3-dione (5 g) in dry dichloromethane (70 ml) during 30 minutes and the reaction mixture stirred at ambient temperature for 4 hours. Triethylamine (15.3 ml) and acetone cyanohydrin (0.5 ml) were added successively and the reaction mixture stirred at ambient temperature for 18 hours. The reaction mixture was washed successively with 2N hydrochloric acid (2×50 ml) and water (2×50 ml), dried over magnesium sulphate and evaporated under reduced pressure to give a yellow glass which was recrystallised from methanol (20 ml) to give 2-(4-methylsulphonyl-2-nitrobenzoyl)-5,5-dimethylcyclohexane-1,3-dione (6.4 g), m.p. 156.5°-158° C., as a yellow crystalline solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05416061 |
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| 出典データセット | uspto-grants-1995_05 |
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| ORD ID | ord-d58fcbdd740644d9af498b7e9b6eb406 |
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| 出典メモ | uspto-grants-1995_05 |
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