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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2086069Generated: October 31, 2026

1-(3-nitrophenyl)pyrrolidin-2-one → 1-(3-Aminophenyl)pyrrolidin-2-one

https://huagongshe.com/reaction/2086069

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-nitrophenyl)pyrrolidin-2-oneHCID 1512870—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1-(3-Aminophenyl)pyrrolidin-2-oneHCID 683956100%

Reaction Steps

A suspension of 1-(3-nitrophenyl)pyrrolidin-2-one (3.0 g, 15 mmol) in ethanol (50 ml) was heated until complete solution was obtained. The solution was cooled to ambient temperature then treated with 10% palladium on charcoal (150 mg) and hydrogenated at 50 psi until hydrogen uptake ceased (ca. 2 hours). The mixture was filtered through a glass microfibre filter paper (Whatman GF/A) and evaporated to dryness to give 1-(3-aminophenyl)pyrrolidin-2-one as a pale green oil (2.6 g, 100%) which was used without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06723735B1
Source datasetuspto-grants-2004_04
ORD IDord-413d825ca72a4efc985dce8771bdc787
Source noteuspto-grants-2004_04