Ammonium Chloride → (S)-3-(2-(4-Fluoro-3-methylphenoxy)acetyl)-4-isopropyloxazolidin-2-one
반응식
[CH:1]([C@H:4]1[CH2:8][O:7][C:6](=[O:9])[NH:5]1)([CH3:3])[CH3:2].[Li]CCCC.[F:15][C:16]1[CH:26]=[CH:25][C:19]([O:20][CH2:21][C:22](Cl)=[O:23])=[CH:18][C:17]=1[CH3:27].[NH4+].[Cl-]>C1COCC1>[F:15][C:16]1[CH:26]=[CH:25][C:19]([O:20][CH2:21][C:22]([N:5]2[C@@H:4]([CH:1]([CH3:3])[CH3:2])[CH2:8][O:7][C:6]2=[O:9])=[O:23])=[CH:18][C:17]=1[CH3:27]참가 물질
반응 조건
- 온도
- -70 °C
실험 절차
To the solution of (S)-( )-4-Isopropyl-2-oxazolidinone (992 mg, 5.6 mmol) in anhydrous 30 mL THF at −70° C. was slowly added n-BuLi (3.5 mL, 5.6 mmol, 1.6 M in hexane) over 15 minutes. The reaction mixture was stirred for 30 min at −70° C. and to it was slowly added a solution of 2-(4-fluoro-3-methylphenoxy)acetyl chloride crude solution in 4 mL THF. The resulting mixture was stirred at −70° C. for 2 h and the temperature was slowly raised over a period of 1 h. The mixture was poured into 30 mL saturated NH4Cl and extracted with ethyl acetate (3×40 mL). The combined organic layers were washed with brine (2×30 mL) and dried over Na2SO4. The solvent was removed under reduced pressure and the product isolated by Flash column chromatography eluting with 0% to 50% ethyl acetate/hexane to give 2.2 g of the title compound as a light yellow oil.
후처리
- customat −70° C.
- customover 15 minutes
- stirringThe resulting mixture was stirred at −70° C. for 2 h
- temperaturethe temperature was slowly raised over a period of 1 h
- extractionextracted with ethyl acetate (3×40 mL)
- washThe combined organic layers were washed with brine (2×30 mL)
- dry with materialdried over Na2SO4
- customThe solvent was removed under reduced pressure
- customthe product isolated by Flash column chromatography
- washeluting with 0% to 50% ethyl acetate/hexane
출처 및 근거
- ORD 기록
- ord-6b6ae7314e0244298e77f214b3caf32b
- 출처 데이터셋
- uspto-grants-2011_02
- 특허 번호
- US07879911B2
반응 노트
불러오는 중…