Ammonia → HCID 21474046, compound
Reaction equation
[NH2:1][C:2]1[CH:11]=[C:10]([N+:12]([O-:14])=[O:13])[C:9]([F: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]([F:15])=[CH:8][C:3]=1[C:4]([NH2:16])=[O:5]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
4.0 g (18.7 mmol) of methyl 2-amino-5-fluoro-4-nitro-benzoate were dissolved in 250 ml of methanol and saturated with ammonia at -40° C. Subsequently, the mixture was stirred at room temperature overnight. The solution was concentrated and ther residue was triturated with methylene chloride. The precipitate was filtered off under suction and dried. 3.17 g (85%) of 2-amino-5-fluoro-4-nitro-benzamide were obtained as yellow crystals;
Workup
- concentrationThe solution was concentrated
- customther residue was triturated with methylene chloride
- filtrationThe precipitate was filtered off under suction
- customdried
Sources & evidence
- ORD record
- ord-1f62b12db0bc4c628c6b6d06335b7b16
- Source dataset
- uspto-grants-1997_11
- Patent number
- US05688803
Reaction notes
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