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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 349816Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/349816

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPivaloyl chlorideHCID 62493—
EduktLithium ChlorideHCID 433294—
Edukt4-Methyl-5-phenyl-2-oxazolidinone, (4S,5R)-HCID 853161—
Edukt3-(2,4-difluorophenyl)propanoic AcidHCID 4986395—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelTriethylamineHCID 8471—
Produkt(4R,5S)-3-[3-(2,4-Difluoro-phenyl)-propionyl]-4-methyl-5-phenyl-oxazolidin-2-oneHCID 6926711099%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07179934B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-dd064df9909948a089c4e4418d5126f0
Quellennotizuspto-grants-2007_02