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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2238546Generated: October 30, 2026

3-Pyridinecarboxaldehyde → 5-Oxo-1-(3-pyridinylmethyl)proline

https://huagongshe.com/reaction/2238546

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-PyridinecarboxaldehydeHCID 10371—
ReactantSodium HydroxideHCID 14798—
ReactantD-Glutamic AcidHCID 23327—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
Product5-Oxo-1-(3-pyridinylmethyl)prolineHCID 1053688761.8%

Reaction Steps

D-glutamic acid (2.21 g, 15 mmol) was dissolved in 2N aqueous sodium hydroxide (15 ml, 30 mmol) at 0° C. and then treated with pyridine-3-carboxaldehyde (1.41 ml, 15 mmol) in ethanol (3 ml). The mixture was stirred at room temperature for 30 minutes and then cooled to 0° C. and treated portion-wise with sodium borohydride (0.189 g, 5 mmol). The mixture was allowed to warm to room temperature with stirring over 4 hrs then after washing with diethyl ether it was acidified to pH5-6 using concentrated hydrochloric acid. The resulting precipitate was collected by filtration, washed with diethyl ether, and dried in vacuo. This material was then taken up in ethanol (50 ml) and refluxed overnight. Fine solids were removed by filtration and then concentration gave 5-oxo-1-(3-pyridinylmethyl)proline (2.04 g) as a white solid which was used without any further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718693B2
Source datasetuspto-grants-2010_05
ORD IDord-08b6525927b24a1cbf1cdbb5737e86e7
Source noteuspto-grants-2010_05