반응식
[Cl:1][C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[CH:4][N:3]=1.OO.NC(N)=[O:13].FC(F)(F)C(OC(=O)C(F)(F)F)=O.O>C(Cl)Cl>[Cl:1][C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[CH:4][N+:3]=1[O-:13]참가 물질
6
실험 절차
To a mixture of 2-chloro-3-methylpyridine (15 g, 118 mmol) and urea hydrogen peroxide (44.07 g, 468.5 mmol) in DCM (300 mL) was added trifluoroacetic anhydride (98.55 g, 469.2 mmol) dropwise at 0° C. The mixture was stirred at room temperature for 20 h. The mixture was then poured into water (150 mL), and the layers were separated. The organic layer was washed with saturated aqueous Na2S2O3 (20 mL), dried over Na2SO4, filtered, and the filtrate was concentrated under reduced pressure. The crude product was purified by silica gel flash chromatography (DCM:MeOH, 100:0 to 10:1) to afford the title compound (14.5 g, 86%) as a colorless solid.
후처리
- customthe layers were separated
- washThe organic layer was washed with saturated aqueous Na2S2O3 (20 mL)
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationthe filtrate was concentrated under reduced pressure
- customThe crude product was purified by silica gel flash chromatography (DCM:MeOH, 100:0 to 10:1)
출처 및 근거
- ORD 기록
- ord-9b19f3851e914078a67b2c5d960f976f
- 출처 데이터셋
- uspto-grants-2016_01
- 특허 번호
- US09227956B2
연결된 노트
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