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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852587Generated: October 30, 2026

Methyl 2-fluoro-5-nitro-3-(2-oxo-1-pyrrolidinyl)benzoate → Methyl 5-amino-2-fluoro-3-(2-oxo-1-pyrrolidinyl)benzoate

https://huagongshe.com/reaction/852587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-fluoro-5-nitro-3-(2-oxo-1-pyrrolidinyl)benzoateHCID 69360218—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductMethyl 5-amino-2-fluoro-3-(2-oxo-1-pyrrolidinyl)benzoateHCID 6935753663%

Reaction Steps

To a solution of methyl 2-fluoro-5-nitro-3-(2-oxo-1-pyrrolidinyl)benzoate (D140) (3.3 g, 11.7 mmol, 1 equiv) in EtOH (100 ml) and H2O (10 ml) were added NH4COOH (7.4 g, 117 mmol, 10 equiv) and 10% palladium on charcoal (50% wet, 660 mg, 10% w/w) and the resulting mixture was refluxed for 2 h then cooled to room temperature. The catalyst was removed by filtration through a pad of celite and most of the solvent removed in vacuo. The residue was partitioned between AcOEt and H2O and the two layers were separated. The organic phase was dried over MgSO4 and concentrated in vacuo to give methyl 5-amino-2-fluoro-3-(2-oxo-1-pyrrolidinyl)benzoate (D150) (1.85 g, 63%) as a pale yellow solid which was used in the next step without further purification. [M+H]+=253.0, RT=2.12 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253198B2
Source datasetuspto-grants-2007_08
ORD IDord-bf5cdfde227f49069ebdcb9cf127f445
Source noteuspto-grants-2007_08