Chlorosuccinimide → 2-Amino-5-chloro-3-nitrobenzamide
反応式
[NH2:1][C:2]1[C:10]([N+:11]([O-:13])=[O:12])=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([NH2:6])=[O:5].[Cl:14]N1C(=O)CCC1=O>C(#N)C>[NH2:1][C:2]1[C:10]([N+:11]([O-:13])=[O:12])=[CH:9][C:8]([Cl:14])=[CH:7][C:3]=1[C:4]([NH2:6])=[O:5]参加物
4
実験手順
2-Amino-3-nitrobenzamide (4.0 g) in warm anhydrous acetonitrile (1.25 L) was treated with N-chlorosuccinimide (3.1 g) at 60° C. under nitrogen for 20 hours. The mixture was allowed to cool to room temperature and filtered. The filter cake was washed with acetonitrile and dried to provide the title compound (3.98 g, 84%). MS (DCI/NH3) m/z 216 (M+H)+.
後処理
- filtrationfiltered
- washThe filter cake was washed with acetonitrile
- customdried
出典と根拠
- ORDレコード
- ord-9504092d5b6c4e348f26e01c38e22ef9
- 出典データセット
- uspto-grants-2012_07
- 特許番号
- US08217070B2
反応ノート
読み込み中…