1-(3-nitrophenyl)-1H-imidazole → 3-(1H-imidazol-1-yl)aniline
反応式
[N:1]1([C:6]2[CH:7]=[C:8]([N+:12]([O-])=O)[CH:9]=[CH:10][CH:11]=2)[CH:5]=[CH:4][N:3]=[CH:2]1.[H][H]>C(O)(=O)C.[Pd]>[N:1]1([C:6]2[CH:7]=[C:8]([CH:9]=[CH:10][CH:11]=2)[NH2:12])[CH:5]=[CH:4][N:3]=[CH:2]1参加物
5
実験手順
To 3-(1-imidazolyl)nitrobenzene (51.6 g, 0.27 mol) in acetic acid (500 ml) is added palladium catalyst (5 g 5% Pd on activated carbon) and the mixture is hydrogenated under pressure (Pstart : 4 bar) until the hydrogen uptake has ceased. The mixture is filtered through celite and the filtrate is evaporated to dryness to leave 2d as a light-brown oil. Yield: 40.4 g (93%).
後処理
- filtrationThe mixture is filtered through celite
- customthe filtrate is evaporated to dryness
出典と根拠
- ORDレコード
- ord-d4f253c2409e4efc896503c132c72194
- 出典データセット
- uspto-grants-1999_07
- 特許番号
- US05922724
反応ノート
読み込み中…