반응식
[NH2:1][C:2]1[CH:3]=[N:4][CH:5]=[CH:6][C:7]=1[O:8][CH3:9].OO.C(OCC)(=O)C.CCCCCC.[ClH:24]>>[NH2:1][C:2]1[C:3]([Cl:24])=[N:4][CH:5]=[CH:6][C:7]=1[O:8][CH3:9]참가 물질
5
실험 절차
To a magnetically stirred mixture of 3-Amino-4-methoxypyridine (4.45 g, 35.89 mmole) in 12N HCl (25 mL) cooled in an ice bath was added hydrogen peroxide (5.3 g, 46.65 mmol, 30% solution). The reaction was allowed to slowly warm to room temperature and stirred for 1 h. TLC (50% ethyl acetate/hexane) indicated complete consumption of starting material. The reaction mixture was slowly poured into saturated sodium bicarbonate solution (400 mL) to neutralize the reaction and extracted with ethyl acetate. The resulting organic layers were washed with saturated sodium chloride solution and dried over magnesium sulfate. Filtration and concentration gave 3-Amino-2-chloro-4 methoxypyridine (4.56 g, 28.77 mmol, 80% yield) as an orange solid.
후처리
- temperaturecooled in an ice bath
- customconsumption of starting material
- additionThe reaction mixture was slowly poured into saturated sodium bicarbonate solution (400 mL)
- customthe reaction
- extractionextracted with ethyl acetate
- washThe resulting organic layers were washed with saturated sodium chloride solution
- dry with materialdried over magnesium sulfate
- filtrationFiltration and concentration
출처 및 근거
- ORD 기록
- ord-2548548e228445b1832b59a62bec1785
- 출처 데이터셋
- uspto-grants-2011_05
- 특허 번호
- US07947692B2
연결된 노트
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