N-bromobutanimide → 6-Bromo-1,2,3,4-tetrahydroquinolin-4-one
반응식
[NH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[C:4](=[O:11])[CH2:3][CH2:2]1.[Br:12]N1C(=O)CCC1=O>ClCCl>[Br:12][C:7]1[CH:6]=[C:5]2[C:10](=[CH:9][CH:8]=1)[NH:1][CH2:2][CH2:3][C:4]2=[O:11]참가 물질
4
실험 절차
To a solution of 2,3-dihydroquinolin-4(1H)-one (2.94 g) in dichloromethane (25 mL) was added N-bromosuccinimide (3.63 g). The mixture was stirred at room temperature for 1.5 h and was partitioned between aqueous sodium bicarbonate and dichloromethane. The organic layer was washed with brine, dried with sodium sulfate, filtered, and concentrated. The concentrate was chromatographed on silica gel using a 35% ethyl acetate in heptane solvent solution and gave 4.14 g of the title compound. MS (ESI−) for C9H8BrNO m/z 225.77 (M−H)−.
후처리
- customwas partitioned between aqueous sodium bicarbonate and dichloromethane
- washThe organic layer was washed with brine
- dry with materialdried with sodium sulfate
- filtrationfiltered
- concentrationconcentrated
- customThe concentrate was chromatographed on silica gel using a 35% ethyl acetate in heptane solvent solution
출처 및 근거
- ORD 기록
- ord-f4bb1526ffa34231af922792372c8e68
- 출처 데이터셋
- uspto-grants-2009_06
- 특허 번호
- US07544717B2
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