反応式
[C:1]1([CH2:7][N:8]2[CH:12]=[N:11][CH:10]=[N:9]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH:13](=[O:17])[CH:14]([CH3:16])[CH3:15]>>[CH2:7]([N:8]1[C:12]([CH:13]([OH:17])[CH:14]([CH3:16])[CH3:15])=[N:11][CH:10]=[N:9]1)[C:1]1[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1参加物
3
実験手順
1-(1-Benzyl-1H-1,2,4-triazol-5-yl)-2-methylpropan-1-ol was synthesized in a manner similar to that of procedure 21 B but using 1-(phenylmethyl)-1H-1,2,4-triazole and isobutyraldehyde as the starting materials. The product was isolated as a white solid in 71% yield.
後処理
- customThe product was isolated as a white solid in 71% yield
出典と根拠
- ORDレコード
- ord-e37f5d0e8162451bb1c32fe29e6c0a00
- 出典データセット
- uspto-grants-2008_07
- 特許番号
- US07399778B2
関連ノート
読み込み中…