反応式
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]=[O:9])=[N:6][CH:7]=1.[BH4-].[Na+]>CO>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][OH:9])=[N:6][CH:7]=1参加物
4
実験手順
To a solution of 5-bromopyridine-2-carbaldehyde (300 mg) in methanol (10 mL) was added sodium borohydride (61 mg) and the reaction stirred at room temperature for 72 h. The reaction was quenched with saturated aqueous sodium carbonate solution (20 mL) and water (20 mL) and extracted into dichloromethane (3×30 mL). The organic layers were dried (MgSO4) and reduced in vacuo to give (5-bromo-pyridin-2-yl)-methanol as a white solid.
後処理
- customThe reaction was quenched with saturated aqueous sodium carbonate solution (20 mL) and water (20 mL)
- extractionextracted into dichloromethane (3×30 mL)
- dry with materialThe organic layers were dried (MgSO4)
出典と根拠
- ORDレコード
- ord-d50072c653d44d7ea55d70ddb7fd33ee
- 出典データセット
- uspto-grants-2013_02
- 特許番号
- US08383620B2
関連ノート
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