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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2392439Generated: October 29, 2026

Benzyl Bromide → (S)-2-benzyl 1-tert-butyl 4-oxopyrrolidine-1,2-dicarboxylate

https://huagongshe.com/reaction/2392439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant(2S)-1-(tert-butoxycarbonyl)-4-oxopyrrolidine-2-carboxylic acidHCID 11593804—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product(S)-2-benzyl 1-tert-butyl 4-oxopyrrolidine-1,2-dicarboxylateHCID 1095814871%

Reaction Steps

To a stirring solution of a mixture of (S)-1-(tert-butoxycarbonyl)-4-oxopyrrolidine-2-carboxylic acid (2.85 g, 12.43 mmol) and potassium carbonate (4.33 g, 24.87 mmol) in anhydrous N,N-dimethylformamide (60 mL) was added benzyl bromide (4.25 g, 24.87 mmol). The mixture was stirred at room temperature overnight. The resulting crude mixture was diluted with ethylacetate and the organic layer was washed with 10% sodium carbonate and brine. The organic layer was dried over sodium sulfate and volatiles were removed in-vacuo. The residue was purified on normal phase column to yield 2.82 g (71%) of desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273341B2
Source datasetuspto-grants-2012_09
ORD IDord-eda151872e134cfead82c0bc30540932
Source noteuspto-grants-2012_09