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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 546615Generated: October 25, 2026

(4-Nitrophenyl)(pyrrolidin-1-yl)methanone → 4-(Pyrrolidin-1-ylcarbonyl)aniline

https://huagongshe.com/reaction/546615

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Nitrophenyl)(pyrrolidin-1-yl)methanoneHCID 386112—
ReactantAmmonium formateHCID 2723923—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product4-(Pyrrolidin-1-ylcarbonyl)anilineHCID 577800115.8%

Reaction Steps

To a solution of 1.28 g of 1-(4-nitrobenzoyl)pyrrolidine obtained in stage a) below in 50 mL of methanol are added, under argon, 4.26 g of ammonium formate and 9 mg of 10% palladium-on-charcoal. The reaction mixture is stirred at room temperature for 5 hours and then filtered through Celite and concentrated under reduced pressure. The residue is taken up in water and extracted with ethyl acetate. The organic phase is then washed with saturated sodium chloride solution, dried over magnesium sulphate, filtered and concentrated under reduced pressure to give 1.28 g of 4-(pyrrolidin-1-ylcarbonyl)aniline, the characteristics of which are as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935819B2
Source datasetuspto-grants-2011_05
ORD IDord-976bb117e69147dfb22da00f6c7266ef
Source noteuspto-grants-2011_05