3-(3-Nitrophenyl)pyridine → 3-(Pyridin-3-yl)aniline
反応式
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([C:7]2[CH:8]=[C:9]([N+:13]([O-])=O)[CH:10]=[CH:11][CH:12]=2)[CH:2]=1>C(O)C.[Ni]>[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([C:7]2[CH:8]=[C:9]([CH:10]=[CH:11][CH:12]=2)[NH2:13])[CH:2]=1参加物
4
実験手順
3-(3-pyridyl)-nitrobenzene (9.1 g, 45.5 mmol) in ethanol (125 ml) is hydrogenated at ambient pressure for 1.75 hours using Raney Nickel as the catalyst. Filtration of the resulting solution through celite followed by evaporation of solvent quantitatively yields 3-(3-pyridyl)aniline.
後処理
- filtrationFiltration of the resulting solution through celite
- customfollowed by evaporation of solvent quantitatively yields 3-(3-pyridyl)aniline
出典と根拠
- ORDレコード
- ord-e2c51de4f901493c8a5c8e21efe583c1
- 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…