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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 2-fluoro-5-nitro-3-(2-oxo-1-pyrrolidinyl)benzoate | HCID 69360218 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 5-amino-2-fluoro-3-(2-oxo-1-pyrrolidinyl)benzoate | HCID 69357536 | 63% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07253198B2 |
|---|
| Source dataset | uspto-grants-2007_08 |
|---|
| ORD ID | ord-bf5cdfde227f49069ebdcb9cf127f445 |
|---|
| Source note | uspto-grants-2007_08 |
|---|