Ammonia → HCID 21474075, Verbindung
Reaktionsgleichung
[NH2:1][C:2]1[CH:11]=[C:10]([N+:12]([O-:14])=[O:13])[C:9]([Br:15])=[CH:8][C:3]=1[C:4](OC)=[O:5].[NH3:16]>CO>[NH2:1][C:2]1[CH:11]=[C:10]([N+:12]([O-:14])=[O:13])[C:9]([Br:15])=[CH:8][C:3]=1[C:4]([NH2:16])=[O:5]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
25.8 g (93.8 mmol) of methyl 2-amino-5-bromo-4-nitro-benzoate were dissolved in 800 ml of methanol and saturated with ammonia at -40° C. Subsequently, the mixture was stirred at room temperature overnight. The solution was concentrated and the residue was triturated with methylene chloride. The precipitate was filtered off under suction and dried. 18.3 g (75%) of 2-amino-5-bromo-4-nitro-benzamide were obtained as orange coloured crystals;
Aufarbeitung
- concentrationThe solution was concentrated
- customthe residue was triturated with methylene chloride
- filtrationThe precipitate was filtered off under suction
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-9b69b947b99b4ce18f1093ce412613ad
- Quelldatensatz
- uspto-grants-1997_11
- Patentnummer
- US05688803
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