Dimethylformamide → Methyl 4-acetyl-2-fluorobenzoate
반응식
[C:1]([C:4]1[CH:12]=[CH:11][C:7]([C:8]([OH:10])=[O:9])=[C:6]([F:13])[CH:5]=1)(=[O:3])[CH3:2].[C:14](Cl)(=O)C(Cl)=O.CN(C)C=O.C(N(CC)CC)C>ClCCl.CO>[C:1]([C:4]1[CH:12]=[CH:11][C:7]([C:8]([O:10][CH3:14])=[O:9])=[C:6]([F:13])[CH:5]=1)(=[O:3])[CH3:2]참가 물질
실험 절차
4-Acetyl-2-fluorobenzoic acid (46.1 mmol, 0.0461 mol) in dichloromethane (30 mL) was treated with oxalyl chloride (7.8 mL, 92 mmol) and N,N-dimethylformamide (0.2 mL) at 0° C. The reaction mixture was stirred at ambient temperature for 3 h. The reaction mixture was concentrated under reduced pressure and the residue was dissolved in dichloromethane (50 mL, 0.78 mol) and cooled to 0° C. A solution of methanol (4.7 mL) and triethylamine (16 mL, 120 mmol) was added. The reaction mixture was stirred at ambient temperature for 1 h, washed with water aqueous 1N hydrochloric acid, and brine. The organic extracts were dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by flash chromatography eluting with 20% ethyl acetate in hexanes to afford the desired product. (5.64 g, 62.4%).
후처리
- concentrationThe reaction mixture was concentrated under reduced pressure
- temperaturecooled to 0° C
- stirringThe reaction mixture was stirred at ambient temperature for 1 h
- washwashed with water aqueous 1N hydrochloric acid, and brine
- dry with materialThe organic extracts were dried over magnesium sulfate
- filtrationfiltered
- concentrationconcentrated under reduced pressure
- customThe residue was purified by flash chromatography
- washeluting with 20% ethyl acetate in hexanes
출처 및 근거
- ORD 기록
- ord-650691fb1d56413db2d5929fc7df21eb
- 출처 데이터셋
- uspto-grants-2010_08
- 특허 번호
- US07767675B2
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