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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359902Generated: October 31, 2026

(S)-4-Benzyl-2-oxazolidinone → (S)-4-Benzyl-3-(2-(4-fluorophenyl)acetyl)oxazolidin-2-one

https://huagongshe.com/reaction/2359902

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-4-Benzyl-2-oxazolidinoneHCID 736225—
Reactant4-Fluorophenylacetyl chlorideHCID 3744988—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(S)-4-Benzyl-3-(2-(4-fluorophenyl)acetyl)oxazolidin-2-oneHCID 155360198,089%

Reaction Steps

To a cooled (−78° C.) solution of (S)-4-benzyloxazolidin-2-one (10.26 g, 58 mmol, 1.0 equiv) in 100 mL THF was added dropwise n-BuLi (40 mL, 1.6 M, 64 mmol, 1.1 equiv). After stirring for 30 minutes, 4-fluorophenylacetyl chloride (10.0 g, 0.58 mmol, 1.0 equiv) was added dropwise. After stirring for an additional 30 minutes, the reaction mixture was allowed to warm to room temperature. The reaction was quenched with sat'd. aq. NH4Cl, extracted with DCM, and washed with brine. The organic layer was then dried over sodium sulfate, filtered, and concentrated in vacuo. Purification by silica gel (10-20% EtOAc/Hexanes) provided the title compound as a thick oil (14.7 g, 81%). m/z=314.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08686007B2
Source datasetuspto-grants-2014_04
ORD IDord-9c5ad317cc6745d8a41c2b32eade429b
Source noteuspto-grants-2014_04