Hydrochloric Acid → 4-[(Benzylamino)methyl]benzonitrile
反応式
C([C:8](=[N:17]O)[C:9]1[CH:16]=[CH:15][C:12]([C:13]#[N:14])=[CH:11][CH:10]=1)C1C=CC=CC=1.Cl>C(O)C>[CH2:8]([NH:17][CH2:8][C:9]1[CH:10]=[CH:11][C:12]([C:13]#[N:14])=[CH:15][CH:16]=1)[C:9]1[CH:16]=[CH:15][CH:12]=[CH:11][CH:10]=1参加物
4
実験手順
3.44 g (15 mmol) of 4-(benzyloximinomethyl)benzonitrile in 120 ml of ethanol are cooled to -15° C. 4.46 g (48 mmol, 4.85 ml) of borane-pyridine complex are then added dropwise in the course of 10 minutes and then 26 ml of ethanolic HCl solution in the course of 20 minutes. After stirring at room temperature for 24 h, the resulting solid is filtered off, dissolved in dichloromethane and the solution is washed with water and sodium hydrogen carbonate solution. The organic phase is dried and concentrated in vacuo.
後処理
- addition4.46 g (48 mmol, 4.85 ml) of borane-pyridine complex are then added dropwise in the course of 10 minutes
- customin the course of 20 minutes
- filtrationthe resulting solid is filtered off
- dissolutiondissolved in dichloromethane
- washthe solution is washed with water and sodium hydrogen carbonate solution
- customThe organic phase is dried
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-bb0550b839ee43c0a9551859d23e1f80
- 出典データセット
- uspto-grants-1997_12
- 特許番号
- US05703050
反応ノート
読み込み中…