Bromoacetic Acid → (4-Fluoro-2-nitro-phenylamino)-acetic acid
Reaction equation
Br[CH2:2][C:3]([OH:5])=[O:4].[F:6][C:7]1[CH:12]=[CH:11][C:10]([NH2:13])=[C:9]([N+:14]([O-:16])=[O:15])[CH:8]=1.[NH4+].[OH-]>C1(C)C(C)=CC=CC=1>[F:6][C:7]1[CH:12]=[CH:11][C:10]([NH:13][CH2:2][C:3]([OH:5])=[O:4])=[C:9]([N+:14]([O-:16])=[O:15])[CH:8]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 120 °C
Procedure
Bromoacetic acid (5.34 g, 32.0 mmol, 0.5 eq) is added dropwise to 4-fluoro-2-nitro-phenylamine (10.0 g, 64.1 mmol, 1.0 eq) at 120° C. After the addition, the reaction mixture is stirred for 2 hours at 120° C. then xylene (10 mL) is added. The resulting reaction mixture is heated at 130° C. for 1 hour, then it is made alkaline with 25% ammonia aqueous solution. Xylene is removed under reduced pressure and the residue is diluted with water (100 mL). The mixture is filtered at 60° C. and the insoluble residue is extracted twice with 10% ammonia aqueous solution at 60° C. The aqueous layer is acidified with hydrochloric acid to pH 5, the precipitated product is filtered, washed with water and ethanol, dried under vacuum to afford (4-fluoro-2-nitro-phenylamino)-acetic acid as a red solid (2.98 g, 34% yield).
Workup
- additionAfter the addition
- customThe resulting reaction mixture
- temperatureis heated at 130° C. for 1 hour
- customXylene is removed under reduced pressure
- additionthe residue is diluted with water (100 mL)
- filtrationThe mixture is filtered at 60° C.
- extractionthe insoluble residue is extracted twice with 10% ammonia aqueous solution at 60° C
- filtrationthe precipitated product is filtered
- washwashed with water and ethanol
- customdried under vacuum
Sources & evidence
- ORD record
- ord-b44ffdcd3d4b43f9b5de26637fba57dd
- Source dataset
- uspto-grants-2014_05
- Patent number
- US08716280B2
Reaction notes
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