Bromine → 2-Bromo-1-(2-fluorophenyl)propan-1-one
反応式
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8](=[O:11])[CH2:9][CH3:10].[Br:12]Br>C(O)(=O)C>[Br:12][CH:9]([CH3:10])[C:8]([C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=1[F:1])=[O:11]参加物
4
実験手順
To a solution of 2′-fluoropropiophenone (25.0 g) in acetic acid (250 mL) was slowly added bromine (8.4 mL). The mixture was stirred at room temperature for 3 hr, and concentrated under reduced pressure. Water (200 mL) was added to the residue, and the mixture was extracted with diisopropyl ether. The extract was washed with saturated aqueous sodium hydrogencarbonate solution, water and saturated brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give the title compound as a yellow oil (yield 36.8 g, 97%).
後処理
- concentrationconcentrated under reduced pressure
- additionWater (200 mL) was added to the residue
- extractionthe mixture was extracted with diisopropyl ether
- washThe extract was washed with saturated aqueous sodium hydrogencarbonate solution, water and saturated brine
- dry with materialdried over anhydrous magnesium sulfate
- filtrationfiltered
- concentrationconcentrated under reduced pressure
出典と根拠
- ORDレコード
- ord-5b35fe2ae44d42db8dea5850c2cd4afe
- 出典データセット
- uspto-grants-2011_07
- 特許番号
- US07977488B2
反応ノート
読み込み中…