反応式
[F:1][C:2]1[CH:3]=[C:4]([C:10](=[O:13])[CH2:11][CH3:12])[CH:5]=[CH:6][C:7]=1[O:8]C.C([O-])([O-])=O.[Na+].[Na+]>Br>[F:1][C:2]1[CH:3]=[C:4]([C:10](=[O:13])[CH2:11][CH3:12])[CH:5]=[CH:6][C:7]=1[OH:8]参加物
4
実験手順
1-(3-Fluoro-4-methoxyphenyl)propan-1-one (421 mg, 2.31 mmol) in 20 mL 40% HBr was refluxed for 1 h., neutralized with solid Na2CO3 at 0° C., and extracted with EtOAc. The extract was washed with brine, dried, concentrated, and purified by column chromatography (eluent: petroleum ether/EtOAc=5/1) over silica gel to give the product (257 mg, 66% yield) as a yellow solid.
後処理
- extractionextracted with EtOAc
- washThe extract was washed with brine
- customdried
- concentrationconcentrated
- custompurified by column chromatography (eluent: petroleum ether/EtOAc=5/1) over silica gel
出典と根拠
- ORDレコード
- ord-bf31d5c70c364868882031a15011a248
- 出典データセット
- uspto-grants-2016_04
- 特許番号
- US09309211B2
関連ノート
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