반응식
[H-].[Na+].[CH2:3]([OH:8])[C:4]([F:7])([F:6])[F:5].[N+]([C:12]1[CH:19]=[CH:18][C:15]([CH:16]=[O:17])=[CH:14][CH:13]=1)([O-])=O>CS(C)=O.[Cl-].[Na+].O>[F:5][C:4]([F:7])([F:6])[CH2:3][O:8][C:12]1[CH:19]=[CH:18][C:15]([CH:16]=[O:17])=[CH:14][CH:13]=1참가 물질
실험 절차
To a stirred suspension of sodium hydride (60% dispersion in mineral oil, 0.87 g, 21.8 mmol) in DMSO (20 ml) was added trifluoroethanol (3.97 g, 39.7 mmol) at 10-15° C. under an atmosphere of argon. The reaction mixture was stirred at this temperature for 20 min then 4-nitrobenzaldehyde (3.0 g, 19.85 mmol) was added in one portion. The reaction mixture was stirred at 10-15° C. for 3 h then at room temperature for 60 h. Brine (100 ml) was added cautiously to the reaction mixture followed by extraction with Et2O (3×70 ml). The combined organic extracts were washed with water, dried (MgSO4) and the solvent removed under reduced pressure to give an oil which was purified by flash chromatography (3:1 Hexane/EtOAc) to give a yellow oil which solidified on standing at room temperature to give the title compound (1.76 g, 43%) as a yellow solid.
후처리
- stirringThe reaction mixture was stirred at 10-15° C. for 3 h
- waitat room temperature for 60 h
- extractionfollowed by extraction with Et2O (3×70 ml)
- washThe combined organic extracts were washed with water
- dry with materialdried (MgSO4)
- customthe solvent removed under reduced pressure
- customto give an oil which
- customwas purified by flash chromatography (3:1 Hexane/EtOAc)
- customto give a yellow oil which
- customon standing at room temperature
출처 및 근거
- ORD 기록
- ord-8188ad2868bb4596b140c3e2cc042c02
- 출처 데이터셋
- uspto-grants-2014_11
- 특허 번호
- US08895313B2
연결된 노트
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