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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434126Generated: October 26, 2026

Benzoyl chloride → (S)-3-benzoyl-4-methyl-2,5-oxazolidinedione

https://huagongshe.com/reaction/434126

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
Reactant4-MethylmorpholineHCID 7972—
Reactant(S)-4-Methyloxazolidine-2,5-dioneHCID 10996998—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventEthyl AcetateHCID 8857—
Product(S)-3-benzoyl-4-methyl-2,5-oxazolidinedioneHCID 985593074%

Reaction Steps

4-Dimethylaminopyridine (61 mg, 0.5 mmol) and N-methylmorpholine (152 mg, 1.5 mmol) were dissolved in ethyl acetate (15 mL), followed by the addition of (S)-4-methyl-2,5-oxazolidinedione (L-alanine-NCA) (230 mg, 2.0 mmol) under ice cooling. Further, a solution of benzoyl chloride (281 mg, 2.0 mmol) in ethyl acetate (7 mL) was added dropwise under ice cooling over 20 minutes. After the resulting mixture was stirred as was at 0° C. for 2 hours, a precipitated salt was filtered off, and the filtrate was concentrated under reduced pressure. The concentration residue was re-dissolved in a mixed solvent consisting of ethyl acetate (5 mL) and hexane (5 mL), and insoluble matter was filtered off. The filtrate was concentrated under reduced pressure to afford the title compound as white crystals (324 mg, 74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06670447B2
Source datasetuspto-grants-2003_12
ORD IDord-96b92b1de51b4a06a7c2e328ae01161c
Source noteuspto-grants-2003_12