関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetone Cyanohydrin | HCID 6406 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 4-Chloro-2-nitrobenzoyl chloride | HCID 10867784 | — |
| 反応物 | 6,6-Dimethylpiperidine-2,4-dione | HCID 12695593 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 3-(4-Chloro-2-nitrobenzoyl)-6,6-dimethylpiperidine-2,4-dione | HCID 19898191 | 62.1% |
反応手順
A solution of 4-chloro-2-nitrobenzoyl chloride (4.4 g) in dry dichloromethane (5 ml) was added at 5°-10° C. to a stirred solution of 6,6-dimethylpiperidine-2,4-dione (2.8 g) and triethylamine (2.8 ml) in dry dichloromethane (50 ml) and the mixture was stirred at ambient temperature for 18 hours. Triethylamine (8.4 ml) and acetone cyanohydrin (0.4 ml) were added successively to the solution and the mixture was stirred at ambient temperature for 4 hours. The resulting solution was washed successively with 2N hydrochloric acid (25 ml) and water (3×25 ml), dried over sodium sulphate and evaporated under reduced pressure to give a yellow solid which was recrystallised from acetonitrile to give 3-(4-chloro-2-nitrobenzoyl)-6,6-dimethylpiperidine-2,4-dione (4 g), mp 162°-162.5° 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 | US05114461 |
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| 出典データセット | uspto-grants-1992_05 |
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| ORD ID | ord-cce4e7944be34b27b9fe87c1ed71c64c |
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| 出典メモ | uspto-grants-1992_05 |
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