N-Iodosuccinimide → HCID 178478182、化合物
反応式
[Cl:1][C:2]1[CH:3]=[C:4]([C:9]2[CH:13]=[CH:12][NH:11][N:10]=2)[CH:5]=[C:6]([Cl:8])[CH:7]=1.C1C(=O)N([I:21])C(=O)C1>ClCCl>[I:21][C:13]1[C:9]([C:4]2[CH:3]=[C:2]([Cl:1])[CH:7]=[C:6]([Cl:8])[CH:5]=2)=[N:10][NH:11][CH:12]=1参加物
4
実験手順
2.13 g (0.01 mol) of 3-(3,5-dichlorophenyl)pyrazole are dissolved, at room temperature and with stirring, in 50 ml of dichloromethane. 2.5 g (0.011 mol) of n-iodosuccinimide are then added and stirring is then continued for 4 days. The reaction mixture is then concentrated, the solid obtained is washed with heptane and boiled in 100 ml of 1N sodium hydroxide. After cooling, the solid is filtered, washed with water and dried to give 2 g (yield 59%, melting point: 170° C.) of 4-iodo-3-(3,5-dichlorophenyl)pyrazole.
後処理
- concentrationThe reaction mixture is then concentrated
- customthe solid obtained
- washis washed with heptane
- temperatureAfter cooling
- filtrationthe solid is filtered
- washwashed with water
- customdried
出典と根拠
- ORDレコード
- ord-a6e693548f194d1cb81482a444275690
- 出典データセット
- uspto-grants-1999_08
- 特許番号
- US05945382
反応ノート
読み込み中…