反応式
[C:1]1([CH2:7][C:8]([NH2:10])=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Br:11]N1C(=O)CCC1=O.O>ClCCl>[Br:11][CH:7]([C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1)[C:8]([NH2:10])=[O:9]参加物
5
実験手順
Benzeneacetamide (3.0 g, 0.022 mol) was dissolved in dichloromethane (60 mL) and N-bromosuccinimide (4.0 g, 0.022 mol) was added. The reaction was stirred at room temperature under UV light for 24 hr. The mixture was poured into water and the layers were separated. The organic layer was washed with water (2×50 mL) then with brine (1×50 mL). The organic layer was dried (magnesium sulfate) then chromatographed on silica (40% ethyl acetate/hexanes) to give 2-Bromo-2-phenylacetamide, compound h Rf 0.37, 40% ethyl acetate/hexanes; MS m/z 216 (M+H).
後処理
- customthe layers were separated
- washThe organic layer was washed with water (2×50 mL)
- dry with materialThe organic layer was dried (magnesium sulfate)
- customthen chromatographed on silica (40% ethyl acetate/hexanes)
出典と根拠
- ORDレコード
- ord-eccf5d443a924dc2b747e9b9781c3046
- 出典データセット
- uspto-grants-2011_11
- 特許番号
- US08058274B2
関連ノート
読み込み中…