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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434132Generated: November 1, 2026

4-Methylmorpholine → (S)-3-(3-phenylpropanoyl)-4-methyl-2,5-oxazolidinedione

https://huagongshe.com/reaction/434132

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantBenzenepropanoyl chlorideHCID 64801—
Reactant(S)-4-Methyloxazolidine-2,5-dioneHCID 10996998—
SolventEthyl AcetateHCID 8857—
Product(S)-3-(3-phenylpropanoyl)-4-methyl-2,5-oxazolidinedioneHCID 5911973155%

Reaction Steps

(S)-4-methyl-2,5-oxazolidinedione (L-alanine-NCA) (345 mg, 3 mmol) was dissolved in ethyl acetate (20 mL), followed by the addition of 3-phenylpropanoyl chloride (658 mg, 3.9 mmol) under ice cooling. Further, a solution of N-methyl-morpholine (394 mg, 3.9 mmol) in ethyl acetate (10 mL) was added dropwise under ice cooling over 20 minutes, and the resulting mixture was then stirred at the same temperature for 2 hours. The reaction mixture was treated in a similar manner as in Synthesis Process 5 of Example 8 to afford the title compound (408 mg, 55%) as a colorless clear syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06670447B2
Source datasetuspto-grants-2003_12
ORD IDord-e4d415af27a24464a60ad98809652090
Source noteuspto-grants-2003_12