m-Nitroacetophenone → 2-Bromo-1-(3-nitrophenyl)ethan-1-one
反応式
[N+:1]([C:4]1[CH:5]=[C:6]([C:10](=[O:12])[CH3:11])[CH:7]=[CH:8][CH:9]=1)([O-:3])=[O:2].[Br-:13].[Br-].[Br-].[NH+]1C=CC=CC=1.[NH+]1C=CC=CC=1.[NH+]1C=CC=CC=1>C(O)(=O)C>[Br:13][CH2:11][C:10]([C:6]1[CH:7]=[CH:8][CH:9]=[C:4]([N+:1]([O-:3])=[O:2])[CH:5]=1)=[O:12]参加物
4
実験手順
m-Nitroacetophenone (20 g) was dissolved in acetic acid (150 mL) under argon. Pyridinium tribromide (38.7 g) was added at once; the reaction was allowed to stir at room temperature for 1 hour and then quenched with water (250 mL). The product was filtered and air dried to give the title compound (25 g, 84%).
後処理
- customquenched with water (250 mL)
- filtrationThe product was filtered
- customair dried
出典と根拠
- ORDレコード
- ord-c14ea3eb512c47819ba451df036c0cd2
- 出典データセット
- uspto-grants-2012_06
- 特許番号
- US08207167B2
反応ノート
読み込み中…