Ethanol → 4-Bromo-3-chloroaniline
反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-])=O)=[CH:4][C:3]=1[Cl:11].CCO.[Cl-].[NH4+].O>C1COCC1.[Fe]>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([NH2:8])=[CH:4][C:3]=1[Cl:11]参加物
反応条件
- 温度
- 60 °C
実験手順
To a solution of 1-bromo-2-chloro-4-nitrobenzene (1.0 g, 4.23 mmol) in THF (7.24 mL) was added EtOH (7.24 mL) followed by ammonium chloride (0.339 g, 6.34 mmol) in water (7.23 mL, 401 mmol) and iron (0.945 g, 16.92 mmol). The reaction mixture was heated at 60° C. in a sealed tube. After 3.5 hours, the reaction mixture was allowed to cool to room temperature and the heterogeneous mixture filtered through a disposable fritted funnel. The filter cake was washed with EtOAc. The solution was concentrated to half-volume, then diluted with EtOAc (10 mL) and 1 N NaOH (10 mL). Layers were separated. Aqueous phase was extracted with EtOAc (3×). The organic phases were combined, dried over Na2SO4, filtered, and concentrated to afford the title compounds as a tan solid. The crude material was used without further purification.
後処理
- temperatureto cool to room temperature
- filtrationthe heterogeneous mixture filtered through a disposable fritted funnel
- washThe filter cake was washed with EtOAc
- concentrationThe solution was concentrated to half-volume
- additiondiluted with EtOAc (10 mL) and 1 N NaOH (10 mL)
- customLayers were separated
- extractionAqueous phase was extracted with EtOAc (3×)
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-fc0d1f2baafb437caad1c82700e081fa
- 出典データセット
- uspto-grants-2014_12
- 特許番号
- US08916553B2
反応ノート
読み込み中…