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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2276735Generated: October 31, 2026

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

https://huagongshe.com/reaction/2276735

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 g, 58 mmol, 1.0 equiv) in 100 mL THF was added dropwise n-BuLi (40 mL, 1.6 M in hexanes, 64 mmol, 1.1 equiv). After stirring for 30 minutes, 4-fluorophenylacetyl chloride (10 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 saturated aq. NH4Cl, extracted with dichloromethane, 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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133123B2
Source datasetuspto-grants-2015_09
ORD IDord-a63c0ee87e4d49cf9ac59ef944a4db88
Source noteuspto-grants-2015_09