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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029672Generated: October 31, 2026

Benzyl Bromide → (S)-Methyl 1-benzyl-5-oxopyrrolidine-2-carboxylate

https://huagongshe.com/reaction/1029672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 5-oxo-L-prolinateHCID 78646—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product(S)-Methyl 1-benzyl-5-oxopyrrolidine-2-carboxylateHCID 10998904—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of methyl (2S)-5-pyrrolidone-2-carboxylate (80 g) in tetrahydrofuran (900 ml) was added sodium hydride (60% in oil, 23.5 g) by portions. After the addition, the reaction mixture was heated to 60° C., and benzyl bromide (69.8 ml) was added dropwise thereto. After 3 hours, the reaction mixture was cooled to room temperature and water (100 ml) was added dropwise thereto. The reaction mixture was poured into a mixture of ethyl acetate (2 l) and water (800 ml). The organic layer was separated, washed with brine, and dried over magnesium sulfate. Evaporation of the solvent gave an oil, which was chromatographed on silica gel (2 l) eluting with a mixture of hexane and ethyl acetate (1:1→1:2, V/V) to give methyl (2S)-1-benzyl-5-pyrrolidone-2-carboxylate (100.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05102877
Source datasetuspto-grants-1992_04
ORD IDord-41ffd208cacf43a09e64464f05c3fe32
Source noteuspto-grants-1992_04