반응식
C[O:2][C:3]1[CH:4]=[C:5]([CH:32]=[CH:33][C:34]=1[O:35]C)[CH:6]=[CH:7][C:8]([NH:10][C:11]1[C:12](=[O:31])[O:13][C:14]2[CH:27]=[C:26]3[CH2:28][CH2:29][CH2:30][C:25]3=[CH:24][C:15]=2[C:16]=1[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=1[CH3:23])=[O:9].[B].C(O)C>ClCCl.O>[OH:2][C:3]1[CH:4]=[C:5]([CH:32]=[CH:33][C:34]=1[OH:35])[CH:6]=[CH:7][C:8]([NH:10][C:11]1[C:12](=[O:31])[O:13][C:14]2[CH:27]=[C:26]3[CH2:28][CH2:29][CH2:30][C:25]3=[CH:24][C:15]=2[C:16]=1[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=1[CH3:23])=[O:9]참가 물질
6
반응물 3
생성물 1
시약·촉매·용매 2
실험 절차
To a solution of 3-(3,4-dimethoxycinnamoylamino)-4-(2-methylphenyl)-7,8-dihydrocylopenta[g][1]benzopyran-2(6H)-one (400 mg) in dichloromethane (6 ml) was added boron tribromidedichloromethane (1:2, 1 ml) dropwise with ice-cooling and stirring. The mixture was further stirred under ice-cooling for 1 hour and, then, added gradually to ethanol (5 ml) with ice-cooling. The mixture was diluted with water and extracted with ethyl acetate, the extract was washed with water and dried (MgSO4), and the solvent was distilled off to give crystals of 3-(3,4-dihydroxycinnamoylamino)-4-(2-methylphenyl)-7,8-dihydrocyclopenta[g][1]benzopyran-2(6H)-one (361 mg, 95.8%). Recrystallization from ethanol gave light brown prisms, m.p. 295°-297° C.
후처리
- temperaturecooling
- stirringThe mixture was further stirred under ice-
- temperaturecooling for 1 hour
- temperaturecooling
- extractionextracted with ethyl acetate
- washthe extract was washed with water
- dry with materialdried (MgSO4)
- distillationthe solvent was distilled off
출처 및 근거
- ORD 기록
- ord-64670c680b504972ae9d8d20c870dae7
- 출처 데이터셋
- uspto-grants-1993_11
- 특허 번호
- US05264454
연결된 노트
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