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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132635Generated: October 26, 2026

Pivaloyl chloride → (4R,5S)-3-[3-(2,4-Difluoro-phenyl)-propionyl]-4-methyl-5-phenyl-oxazolidin-2-one

https://huagongshe.com/reaction/132635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPivaloyl chlorideHCID 62493—
ReactantLithium ChlorideHCID 433294—
Reactant4-Methyl-5-phenyl-2-oxazolidinone, (4S,5R)-HCID 853161—
Reactant3-(2,4-difluorophenyl)propanoic AcidHCID 4986395—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
Product(4R,5S)-3-[3-(2,4-Difluoro-phenyl)-propionyl]-4-methyl-5-phenyl-oxazolidin-2-oneHCID 6926711099%

Reaction Conditions

Temperature0 °C

Reaction Steps

A flask was charged with 29.5 g (158 mmol) of 3-(2,4-difluoro-phenyl)-propionic acid, 700 mL of THF, and 82.8 mL of triethylamine. The mixture was cooled to 0° C. and 23.4 mL of trimethyl acetyl chloride was added slowly. The mixture was stirred cold for 1 hour. Then 8.06 g (190 mmol) of LiCl and 28.1 g of (4S,5R)-4-methyl-5-phenyl-oxazolidin-2-one was added. The mixture was allowed to warm room temperature and stirred overnight. The solids were filtered off, and the solvent was removed under reduced pressure. The residue was taken up in diethyl ether and washed with sat. aq. ammonium chloride, sat. aq. sodium bicarbonate, and the solvent was removed under reduced pressure. The crude residue was purified by column chromatography (3:1 dichloromethane/hexanes eluent) to give 54 g (99% yield) of the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07388023B2
Source datasetuspto-grants-2008_06
ORD IDord-5aab9024ad7c4aac9a0a584ae2318b23
Source noteuspto-grants-2008_06