反応式
[Br:1]Br.[CH3:3][O:4][C:5]1[CH:12]=[CH:11][CH:10]=[CH:9][C:6]=1[C:7]#[N:8]>C(Cl)(Cl)Cl>[Br:1][C:10]1[CH:11]=[CH:12][C:5]([O:4][CH3:3])=[C:6]([CH:9]=1)[C:7]#[N:8]参加物
4
実験手順
Bromine (13.7 g, 86.0 mmol) in CHCl3 (20 mL) was added to a solution of 2-(methyloxy)benzonitrile (10.9 g, 81.9 mmol) in CHCl3 (50 mL). The mixture was refluxed for 29 h. The reaction was allowed to cool to room temperature, and washed with saturated sodium bisulfite (50 mL), and brine (50 mL). The organic layer was dried over anhydrous sodium sulfate. Evaporation of the solvent afforded 5-bromo-2-(methyloxy)benzonitrile (12.4 g, 71%).
後処理
- temperatureThe mixture was refluxed for 29 h
- washwashed with saturated sodium bisulfite (50 mL), and brine (50 mL)
- dry with materialThe organic layer was dried over anhydrous sodium sulfate
- customEvaporation of the solvent
出典と根拠
- ORDレコード
- ord-91481a9d681b44488b6800dcaf7e00da
- 出典データセット
- uspto-grants-2011_12
- 特許番号
- US08071588B2
関連ノート
読み込み中…