Ethanol → Ethyl 2-(4-fluorophenyl)-2-hydroxyacetate
반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([OH:12])[C:9]([OH:11])=[O:10])=[CH:4][CH:3]=1.OS(O)(=O)=O.[CH2:18](O)[CH3:19]>>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]([OH:12])[C:9]([O:11][CH2:18][CH3:19])=[O:10])=[CH:6][CH:7]=1참가 물질
실험 절차
To a cooled solution of 2-(4-fluorophenyl)-2-hydroxyacetic acid (5.0 g, 29.4 mmol) in ethanol was added con. H2SO4 (10 mL) over a period of 10 min. The reaction mixture was heated at reflux for 5 h. The solvent was evaporated under reduced pressure and the residue was diluted with ethyl acetate (25 mL). The organic solution was washed with aqueous saturated NaHCO3 (25 mL×2), water (20 mL), brine solution (10 mL), dried over anhydrous Na2SO4 and evaporated under reduced pressure to give ethyl 2-(4-fluorophenyl)-2-hydroxyacetate (5.0 g, 90%) as crude compound (oily liquid). The crude compound was taken to the next step without further purification. LC-MS (M+H2O)+=216. 1H NMR (400 MHz, DMSO-d6): δ 7.43-7.46 (2H, m), 7.17-7.20 (2H, m), 6.11-6.13 (1H, m), 5.14 (1H, d, J=5.20 Hz), 3.35-4.13 (2H, m), 1.12-1.15 (3H, m).
후처리
- temperatureThe reaction mixture was heated
- temperatureat reflux for 5 h
- customThe solvent was evaporated under reduced pressure
- additionthe residue was diluted with ethyl acetate (25 mL)
- washThe organic solution was washed with aqueous saturated NaHCO3 (25 mL×2), water (20 mL), brine solution (10 mL)
- dry with materialdried over anhydrous Na2SO4
- customevaporated under reduced pressure
출처 및 근거
- ORD 기록
- ord-cc30f38b58a04e548a023b7a8d59a270
- 출처 데이터셋
- uspto-grants-2014_01
- 특허 번호
- US08637525B2
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