Methanol → Methyl 4-(4-fluoro-3-methylphenyl)-4-oxobutanoate
反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:14])[CH2:9][CH2:10][C:11]([OH:13])=[O:12])=[CH:4][C:3]=1[CH3:15].OS(O)(=O)=O.[CH3:21]O>>[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:14])[CH2:9][CH2:10][C:11]([O:13][CH3:21])=[O:12])=[CH:4][C:3]=1[CH3:15]参加物
4
実験手順
To the crude 4-(4-fluoro-3-methyl-phenyl)-4-oxo-butyric acid in 50 mL methanol was added 500 μL concentrated H2SO4 at 25° C. After stirring for 16 h, the mixture was concentrated under reduced pressure and 50 mL water was added. The mixture was extracted with ethyl acetate (3×50 mL) and the combined organic layers washed with brine (2×30 mL) and the product isolated using silica gel chromatography to afford 1.2 g of the title compound as a colorless oil.
後処理
- concentrationthe mixture was concentrated under reduced pressure and 50 mL water
- additionwas added
- extractionThe mixture was extracted with ethyl acetate (3×50 mL)
- washthe combined organic layers washed with brine (2×30 mL)
- customthe product isolated
出典と根拠
- ORDレコード
- ord-840db33ff633417581ab633bf255edfd
- 出典データセット
- uspto-grants-2012_02
- 特許番号
- US08119692B2
反応ノート
読み込み中…