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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554116Generated: October 26, 2026

Benzaldehyde → (S)-1-Benzyl-5-carboxy-2-pyrrolidinone

https://huagongshe.com/reaction/554116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSodium HydroxideHCID 14798—
ReactantD-Glutamic AcidHCID 23327—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
Product(S)-1-Benzyl-5-carboxy-2-pyrrolidinoneHCID 10900113—

Reaction Conditions

Temperature0 °C

Reaction Steps

D-glutamic acid (1.47 g, 10 mmol) was dissolved in 2N aqueous sodium hydroxide (10 ml, 20 mmol) and stirred for 15 minutes. The mixture was then treated with a solution of benzaldehyde (1.1 ml, 10 mmol) in ethanol (3 ml) and stirred at room temperature for 30 minutes. The mixture was cooled to 0° C. and treated with sodium borohydride (0.030 g). The mixture was allowed to warm to room temperature with stirring over 4 hrs and then washed with diethyl ether (three times) before acidifying with concentrated hydrochloric acid to pH2. The resulting precipitate was filtered off and washed with diethyl ether before slurrying in ethanol and azeotroping three times with more ethanol. Finally the remaining material was slurried in ethanol (50 ml) and heated at reflux for 16 hrs. The mixture was then cooled to room temperature and evaporated in vacuo. Drying afforded pure 5-oxo-1-(phenylmethyl)proline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08048907B2
Source datasetuspto-grants-2011_11
ORD IDord-1898bb4dc3dc4c5ebc60dac149dd3dee
Source noteuspto-grants-2011_11