Hydrochloric Acid → N-(5-Acetylamino-2-methyl-phenyl)-2,2,2-trifluoro-acetamide
반응식
[NH2:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:15])=[C:6]([NH:8][C:9](=[O:14])[C:10]([F:13])([F:12])[F:11])[CH:7]=1.N1C=CC=CC=1.[C:22](Cl)(=[O:24])[CH3:23].Cl>CCCCCC.C(OCC)(=O)C.C(Cl)Cl>[C:22]([NH:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:15])=[C:6]([NH:8][C:9](=[O:14])[C:10]([F:11])([F:12])[F:13])[CH:7]=1)(=[O:24])[CH3:23]참가 물질
반응 조건
- 온도
- 0 °C
실험 절차
N-(5-Amino-2-methyl-phenyl)-2,2,2-trifluoro-acetamide (3.27 gm 14.99 mmol) was taken up on anhydrous DCM (75 mL) and cooled to 0° C. Pyridine (3.56 g, 44.97 mmol, 3.64 mL) was added followed by a slow addition of acetyl chloride (1.18 g, 14.99 mol, 1.07 mL). The reaction was allowed to warm to room temp and stir for 30 min. The reaction mixture poured into 1N HCl and the aqueous layer was extracted three times with ethyl acetate. The combined organic layers were washed with saturated sodium bicarbonate, water, brine and dried over anhydrous magnesium sulfate. The solution was filtered and the solvent removed under reduced pressure. The product was isolated by flash chromatography. (3:1 hexane/ethyl acetate) Yield 2.93 g. 1H NMR (CDCl3, 300 MHz) δ 2.13 (s, 3H), 2.23 (s, 3H), 7.25 (d, J=9 Hz, 1H), 7.23 (d, J=9 Hz, 1H), 7.61 (s, 1H).
후처리
- temperatureto warm to room temp
- extractionthe aqueous layer was extracted three times with ethyl acetate
- washThe combined organic layers were washed with saturated sodium bicarbonate, water, brine
- dry with materialdried over anhydrous magnesium sulfate
- filtrationThe solution was filtered
- customthe solvent removed under reduced pressure
- customThe product was isolated by flash chromatography
출처 및 근거
- ORD 기록
- ord-4e5752271d6745a3873e46d02b71ad4e
- 출처 데이터셋
- uspto-grants-2005_06
- 특허 번호
- US06906067B2
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