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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013831Generated: November 1, 2026

(R)-4-Benzyl-2-oxazolidinone → (R)-4-Benzyl-3-pent-4-enoyloxazolidin-2-one

https://huagongshe.com/reaction/1013831

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-4-Benzyl-2-oxazolidinoneHCID 2734969—
Reactant4-Pentenoyl chlorideHCID 4228493—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(R)-4-Benzyl-3-pent-4-enoyloxazolidin-2-oneHCID 10858190—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Dissolve (R)-4-Benzyl-2-oxazolidinone (5.906 g, 33.33 mmoles) and 4-Pentenoyl chloride (4.54 g, 38.33 mmoles) in THF (50 mL). Cool the mixture in a dry ice acetone bath, and add n-Butyl Lithium (36.66 mmoles; 14.66 mL; 10.12 g) dropwise at −78° C. Stir the mixture at −78° C. for 30 min and then warm to ambient temperature. Quench the solution with 60 ml of sat. ammonium chloride, and then extract with 60 ml MTBE. Separate the organics and dry over magnesium sulfate. Filter the drying agent and concentrate under vacuum to an oil (6.96 g). LCMS=100% 260 amu (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981918B2
Source datasetuspto-grants-2011_07
ORD IDord-445ebb5b678248ffb3d2c1117c6c1cd5
Source noteuspto-grants-2011_07