Sodium borohydride → 1-(6-Chloropyrimidin-4-yl)ethanol
反応式
[Cl:1][C:2]1[N:7]=[CH:6][N:5]=[C:4]([C:8](=[O:10])[CH3:9])[CH:3]=1.[BH4-].[Na+]>C(O)C>[Cl:1][C:2]1[N:7]=[CH:6][N:5]=[C:4]([CH:8]([OH:10])[CH3:9])[CH:3]=1参加物
4
実験手順
1-(6-Chloro-4-pyrimidinyl)ethanone (Intermediate 18A, 1.0 g, 6.39 mmol) was dissolved in ethanol (21 mL), treated with sodium borohydride (0.242 g, 6.39 mmol) and the resulting mixture was stirred at room temperature under argon for 2 hours. The solvent was removed under reduced pressure and the residue was diluted with water and extracted with ethyl acetate (×3). The ethyl acetate layers were combined, dried under magnesium sulfate and evaporated under reduced pressure to give the title compound as a yellow oil (808 mg);
後処理
- customThe solvent was removed under reduced pressure
- additionthe residue was diluted with water
- extractionextracted with ethyl acetate (×3)
- customdried under magnesium sulfate
- customevaporated under reduced pressure
出典と根拠
- ORDレコード
- ord-e2acdec75d9640a7ac4fac48b35ea0e7
- 出典データセット
- uspto-grants-2014_08
- 特許番号
- US08796283B2
反応ノート
読み込み中…