Ammonia → 2-Fluoro-6-hydroxybenzamide
Reaction equation
[F:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]([OH:11])[C:3]=1[C:4](O)=[O:5].C(Cl)(=O)C(Cl)=O.[NH3:18].C(=O)(O)[O-].[Na+]>C(OCC)(=O)C.CN(C)C=O>[F:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]([OH:11])[C:3]=1[C:4]([NH2:18])=[O:5]Participants
Conditions
- Temperature
- 0 °C
Procedure
2-Fluoro-6-hydoxybenzoic acid (20.0 g, 0.128 mol) and oxalyl chloride (22.3 ml, 0.256 mol) were dissolved in ethyl acetate (300 ml) together with N,N-dimethylformamide (DMF) (2 drops) and the mixture was stirred under an atmosphere of nitrogen for 20 h. The solvent was removed by distillation under reduced pressure leaving the crude acid chloride which was redissolved in ethyl acetate (300 ml) and cooled to 0° C. Concentrated aqueous ammonia (d 0.88, 50 ml) was added dropwise and the mixture was stirred for a further 2 h. The mixture was poured into aqueous sodium bicarbonate solution. The organic phase was separated and the aqueous phase extracted with ethyl acetate (2×200 ml). The combined organic phases were dried (MgSO4) and concentrated leaving the crude compound (10.2 g, 51.5%). Mass spectrum (-ve CI)m /z 154 (M+ -H) .
Workup
- customThe solvent was removed by distillation under reduced pressure
- customleaving the crude acid chloride which
- stirringthe mixture was stirred for a further 2 h
- customThe organic phase was separated
- extractionthe aqueous phase extracted with ethyl acetate (2×200 ml)
- dry with materialThe combined organic phases were dried (MgSO4)
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-bb541e09b10f4699bcb71326bd6242fc
- Source dataset
- uspto-grants-2000_08
- Patent number
- US06100246
Reaction notes
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