참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetone Cyanohydrin | HCID 6406 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 4-Chloro-2-nitrobenzoyl chloride | HCID 10867784 | — |
| 반응물 | 6,6-Dimethylpiperidine-2,4-dione | HCID 12695593 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 3-(4-Chloro-2-nitrobenzoyl)-6,6-dimethylpiperidine-2,4-dione | HCID 19898191 | 62.1% |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05114461 |
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| 출처 데이터셋 | uspto-grants-1992_05 |
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| ORD ID | ord-cce4e7944be34b27b9fe87c1ed71c64c |
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| 출처 메모 | uspto-grants-1992_05 |
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