반응식
[NH2:1][C:2]1[CH:7]=[C:6]([C:8]([O:10][CH3:11])=[O:9])[CH:5]=[CH:4][C:3]=1[OH:12].C(OCC)(=O)C.C(=O)([O-])O.[Na+].Br[C:25]([CH3:30])([CH3:29])[C:26](Br)=[O:27]>O>[CH3:29][C:25]1([CH3:30])[C:26](=[O:27])[NH:1][C:2]2[CH:7]=[C:6]([C:8]([O:10][CH3:11])=[O:9])[CH:5]=[CH:4][C:3]=2[O:12]1참가 물질
실험 절차
To solution of 2-amino-4-methoxycarbonylphenol [Acta Chimica Academiae Scientiarum Hungaricae, 99 (1), 49-50 (1979)] (4.78 g) in a mixed solvent of ethyl acetate (50 ml) and water (50 ml) were added sodium hydrogen carbonate (3.6 g) and 2-bromoisobutyryl bromide (6.90 g) and the mixture was stirred at room temperature for 10 minutes. The organic layer was separated and the solvent was distilled off under reduced pressure. The resulting residue was dissolved in dimethylformamide (70 ml), to the solution was added potassium carbonate (4.35 g) and the mixture was stirred at room temperature for a day. The reaction solution was poured into water to give precipitates, which were taken by filtration and dried to give 2,2-dimethyl-6-methoxycarbonyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazine (5.4 g).
후처리
- customThe organic layer was separated
- distillationthe solvent was distilled off under reduced pressure
- dissolutionThe resulting residue was dissolved in dimethylformamide (70 ml), to the solution
- additionwas added potassium carbonate (4.35 g)
- stirringthe mixture was stirred at room temperature for a day
- additionThe reaction solution was poured into water
- customto give
- customprecipitates
- filtrationwhich were taken by filtration
- customdried
출처 및 근거
- ORD 기록
- ord-c62b92fd63cc49bab014604fcad2e63b
- 출처 데이터셋
- uspto-grants-1997_01
- 특허 번호
- US05597820
연결된 노트
불러오는 중…