Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54469Generated: October 25, 2026

Ammonium formate → 2-(Pyrrolidin-3-yl)pyridine

https://huagongshe.com/reaction/54469

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant2-(1-Benzylpyrrolidin-3-yl)pyridineHCID 10955622—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2-(Pyrrolidin-3-yl)pyridineHCID 501393875%

Reaction Steps

To a suspension of 2-[1-(phenylmethyl)-3-pyrrolidinyl]pyridine (7.15 g, 30.0 mmol) and 10% palladium on charcoal catalyst (1.90 g) in methanol (120 mL) was added dropwise a solution of ammonium formate (7.57 g, 120 mmol) in water (30 mL). The mixture was heated at reflux for 30 minutes, allowed to cool to room temperature, and filtered. The filtrate was concentrated under reduced pressure, the residue was taken up in water (10 mL), and the solution was made basic with concentrated ammonia and extracted with dichloromethane (4×15 mL). The organic extracts were combined, dried over anhydrous potassium carbonate, and concentrated to a yellow oil. This crude product was chromatographed (silica gel, chloroform-methanol-ammonia 75:25:5) to give the title compound (3.33 g, 75%) as a faint yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05622966
Source datasetuspto-grants-1997_04
ORD IDord-d9df612e9c6a45d9938703ca0ca2de1f
Source noteuspto-grants-1997_04