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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580561Generated: October 30, 2026

Benzyl Bromide → Ethyl 1-benzyl-3-methyl-2-oxo-4-pyrrolidinecarboxylate

https://huagongshe.com/reaction/580561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
Reactant3-Pyrrolidinecarboxylic acid, 4-methyl-5-oxo-, ethyl esterHCID 12292463—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl 1-benzyl-3-methyl-2-oxo-4-pyrrolidinecarboxylateHCID 1393313380.7%

Reaction Steps

To a suspension of sodium hydride (2.30 g) in absolute dioxane (100 ml) was added dropwise ethyl 3-methyl-2-oxo-4-pyrrolidinecarboxylate (13.68 g) with stirring at room temperature. After stirring for 30 minutes, to a reaction mixture was added benzylbromide (16.42 g) during 20 minutes, then stirred for 2 hours and allowed to stand overnight at room temperature. The reaction mixture was poured into ice-water (100 ml) and extracted with chloroform, washed with water, dried over anhydrous sodium sulfate and concentrated. The residue was purified by vacuum distillation to give ethyl 1-benzyl-3-methyl-2-oxo-4-pyrrolidinecarboxylate (16.86 g), bp 155°-185° C./2 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04753953
Source datasetuspto-grants-1988_06
ORD IDord-8c8038e0da9e497b87dd3f02971af5a3
Source noteuspto-grants-1988_06