反応式
[CH3:1][NH:2][C:3]1[CH:11]=[CH:10][C:6]([C:7](O)=[O:8])=[CH:5][C:4]=1[N+:12]([O-:14])=[O:13].S(Cl)([Cl:17])=O>>[CH3:1][NH:2][C:3]1[CH:11]=[CH:10][C:6]([C:7]([Cl:17])=[O:8])=[CH:5][C:4]=1[N+:12]([O-:14])=[O:13]参加物
3
反応条件
- 温度
- 80 °C
実験手順
4-Methylamino-3-nitro-benzoyl chloride (4.3 g) was prepared starting from 4-methylamino-3-nitro-benzoic acid (4 g) in thionyl chloride (20 mL). The reaction was heated to 80° C. for 8 h. The solvent was evaporated to isolate pure compound without any further purification.
後処理
- customThe solvent was evaporated
- customto isolate pure compound
- customwithout any further purification
出典と根拠
- ORDレコード
- ord-cf67af8299fd443997516bc33d342552
- 出典データセット
- uspto-grants-2014_06
- 特許番号
- US08759535B2
関連ノート
読み込み中…