반응식
[H-].[Na+].[CH3:3][N:4]1[CH2:8][CH2:7][NH:6][C:5]1=[C:9]([N+:13]([O-:15])=[O:14])[C:10]([OH:12])=[O:11].[Cl:16][C:17]1[CH:27]=[C:26]([Cl:28])[CH:25]=[CH:24][C:18]=1[O:19][CH2:20][C:21](Cl)=[O:22].[CH3:29]N(C)C=O>>[CH3:29][O:11][C:10](=[O:12])[C:9](=[C:5]1[N:4]([CH3:3])[CH2:8][CH2:7][N:6]1[C:21](=[O:22])[CH2:20][O:19][C:18]1[CH:24]=[CH:25][C:26]([Cl:28])=[CH:27][C:17]=1[Cl:16])[N+:13]([O-:15])=[O:14]참가 물질
실험 절차
2.3 g of sodium hydride was slurried in 75 ml of dimethylformamide at 5°. To that slurry, at 5°, was added 19.5 g of 1B over a 30-minute period. The stirred mixture was allowed to warm to room temperature and stirred at that temperature for one hour. The mixture then was cooled to 5° and there was added thereto a solution of 25.5 g of 2,4-dichlorophenoxyacetyl chloride in 25 ml of dimethylformamide, over a 20-minute period, the stirred mixture being held at 5°-12°. The stirred mixture was allowed to warm to room temperature and stirred at that temperature overnight. The mixture then was poured into ice water. The solid was filtered, washed with water and dried by air aspiration and ether washing to give a tan-colored solid, which on recrystallization from acetonitrile gave 1, as an off-white solid, m.p.; 191°-192° (with decomposition).
후처리
- temperatureThe mixture then was cooled to 5°
- additionthere was added
- custombeing held at 5°-12°
- temperatureto warm to room temperature
- stirringstirred at that temperature overnight
- filtrationThe solid was filtered
- washwashed with water
- dry with materialdried by air aspiration and ether washing
- customto give a tan-colored solid, which
- customon recrystallization from acetonitrile
- customgave 1
출처 및 근거
- ORD 기록
- ord-23f428c50188440e862d78e2954b53b6
- 출처 데이터셋
- uspto-grants-1977_10
- 특허 번호
- US04052411
연결된 노트
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