Imidazole → 2-Hydroxy-4-imidazol-1-ylmethyl-benzonitrile
反応式
Br[CH2:2][C:3]1[CH:10]=[CH:9][C:6]([C:7]#[N:8])=[C:5]([OH:11])[CH:4]=1.[NH:12]1[CH:16]=[CH:15][N:14]=[CH:13]1>CN(C=O)C>[OH:11][C:5]1[CH:4]=[C:3]([CH2:2][N:12]2[CH:16]=[CH:15][N:14]=[CH:13]2)[CH:10]=[CH:9][C:6]=1[C:7]#[N:8]参加物
4
実験手順
4-bromomethyl-2-hydroxy-benzonitrile (0.22 g, 1.05 mmol) and imidazole (0.36 g, 5.23 mmol) were dissolved in DMF (10 mL) with stirring at ambient temperature. After stirring for 18 h, the reaction mixture was concentrated in vacuo and purified by silica gel chromatography eluting with 2% CH3OH/CH2C12 to 5% CH3OH/CH2Cl2 to give the title compound.
後処理
- stirringAfter stirring for 18 h
- concentrationthe reaction mixture was concentrated in vacuo
- custompurified by silica gel chromatography
- washeluting with 2% CH3OH/CH2C12 to 5% CH3OH/CH2Cl2
出典と根拠
- ORDレコード
- ord-b0d36694988949c584188e150db9557d
- 出典データセット
- uspto-grants-2001_10
- 特許番号
- US06297239B1
反応ノート
読み込み中…