2-(2-chloro-5-nitrophenyl)-5-phenyl-1H-imidazole → 4-Chloro-3-(5-phenyl-1H-imidazol-2-yl) aniline
反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-])=O)=[CH:4][C:3]=1[C:11]1[NH:12][C:13]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)=[CH:14][N:15]=1>CCO>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([NH2:8])=[CH:4][C:3]=1[C:11]1[NH:12][C:13]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)=[CH:14][N:15]=1参加物
実験手順
To a solution of 2-(2-chloro-5-nitrophenyl)-5-phenyl-1H-imidazole (27 g, 90.3 mmol) in EtOH (200 ml) is added 5 nCl2.2H2O (71 g, 316 mmol). The mixture is refluxed for 2 hours, cooled to room temperature and then concentrated. Ethyl acetate (200 ml) and NaOH (25 g in 100 ml water) are added to the residue and the mixture is stirred for 10 minutes at room temperature. The solid is removed by filtering through celite pad. The filtrate is separated and the organic layer is further washed with brine, dried over anhydrous MgSO4 and concentrated. The crude product is purified by silica gel flash chromatography, eluted with 40% ethyl acetate in dichloromethane to afford 4-Chloro-3-(5-phenyl-1H-imidazol-2-yl) aniline as a brown solid. LC-MS m/z: 270.1 (M+1).
後処理
- temperatureThe mixture is refluxed for 2 hours
- concentrationconcentrated
- additionEthyl acetate (200 ml) and NaOH (25 g in 100 ml water) are added to the residue
- customThe solid is removed
- filtrationby filtering through celite pad
- customThe filtrate is separated
- washthe organic layer is further washed with brine
- dry with materialdried over anhydrous MgSO4
- concentrationconcentrated
- customThe crude product is purified by silica gel flash chromatography
- washeluted with 40% ethyl acetate in dichloromethane
出典と根拠
- ORDレコード
- ord-0a9e2c336d86421f92c5cdeac8cd5c0c
- 出典データセット
- uspto-grants-2015_12
- 特許番号
- US09216964B2
反応ノート
読み込み中…