반응식
[S:1]1[CH2:6][CH2:5][C:4](=[O:7])[CH2:3][CH2:2]1.[N+:8]([CH3:11])([O-:10])=[O:9]>C(O)C.C[O-].[Na+]>[N+:8]([CH2:11][C:4]1([OH:7])[CH2:5][CH2:6][S:1][CH2:2][CH2:3]1)([O-:10])=[O:9]참가 물질
실험 절차
Under a nitrogen atmosphere sodium methoxide (1.03 mL of 25 wt % in methanol, 4.51 mmol) was added dropwise to a solution of tetrahydro-4H-thiopyran-4-one (10.48 g, 90.20 mol) and nitromethane (7.33 mL, 135.3 mmol) in ethanol (6 mL). The reaction mixture was stirred at ambient temperature for 5 days and then concentrated under reduced pressure. The residue was partitioned between chloroform (400 mL) and water (60 mL). The aqueous was extracted with chloroform (5×100 mL). The combined organics were dried over magnesium sulfate, filtered, and then concentrated under reduced pressure. The residue was purified by HPFC eluting with a gradient of 3-35% ethyl acetate in hexanes to provide 10.23 g of 4-(nitromethyl)tetrahydro-2H-thiopyran-4-ol.
후처리
- concentrationconcentrated under reduced pressure
- customThe residue was partitioned between chloroform (400 mL) and water (60 mL)
- extractionThe aqueous was extracted with chloroform (5×100 mL)
- dry with materialThe combined organics were dried over magnesium sulfate
- filtrationfiltered
- concentrationconcentrated under reduced pressure
- customThe residue was purified by HPFC
- washeluting with a gradient of 3-35% ethyl acetate in hexanes
출처 및 근거
- ORD 기록
- ord-a8faff76167a49a6a932dbb483511e5f
- 출처 데이터셋
- uspto-grants-2013_09
- 특허 번호
- US08541438B2
연결된 노트
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