Hydrazine hydrate (1:1) → Methyl 2-chloro-3-hydrazinocarbonyl-4-methylsulfonylbenzoate
反応式
[Cl:1][C:2]1[C:11]([C:12](Cl)=[O:13])=[C:10]([S:15]([CH3:18])(=[O:17])=[O:16])[CH:9]=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5].O.[NH2:20][NH2:21]>C(Cl)Cl>[Cl:1][C:2]1[C:11]([C:12]([NH:20][NH2:21])=[O:13])=[C:10]([S:15]([CH3:18])(=[O:17])=[O:16])[CH:9]=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5]参加物
4
実験手順
At room temperature, 3.11 g (10 mmol) of methyl 2-chloro-3-chloroformyl-4-methylsulfonylbenzoate in 50 ml of methylene chloride were added dropwise to 1.0 g (20 mmol) of hydrazine hydrate in 30 ml of methylene chloride. The reaction mixture was stirred at room temperature for 1 hour and then washed with water, dried and concentrated. 1.2 g (39% of theory) of methyl 2-chloro-3-hydrazinocarbonyl-4-methylsulfonylbenzoate were obtained.