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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366367Generated: October 30, 2026

3-Cyclopentylpropionyl chloride → (4S)-benzyl-3-(3-cyclopentylpropanoyl)oxazolidin-2-one

https://huagongshe.com/reaction/1366367

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Cyclopentylpropionyl chlorideHCID 66039—
Reactant(S)-4-Benzyl-2-oxazolidinoneHCID 736225—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(4S)-benzyl-3-(3-cyclopentylpropanoyl)oxazolidin-2-oneHCID 11077479100%

Reaction Steps

To a solution of (S)-(−)-4-benzyl-2-oxazolidinone (25 g, 141 mmol) in THF (350 mL) at −78° C. was added dropwise n-BuLi (56.4 mL, 2.5M solution in hexane, 141 mmol). After stirring for 60 min at the same temperature, the reaction mixture was then treated with 3-cyclopentylpropionyl chloride (21.6 mL, 141 mmol) over 0.25 h. The reaction mixture was allowed to warm to room temperature and stirred overnight. The reaction was quenched with saturated aqueous NH4Cl solution (320 mL). The aqueous layer was extracted with EtOAc (3×200 mL). The combined organic layers were dried (MgSO4) and evaporated to yield (4S)-benzyl-3-(3-cyclopentylpropanoyl)oxazolidin-2-one as a white solid (42.4 g, 100%). LCMS: (M+H)+: 302.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893056B2
Source datasetuspto-grants-2011_02
ORD IDord-7adf4436787242a7bcd1b248efe2099f
Source noteuspto-grants-2011_02