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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 349816생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/349816

반응식

참여 물질

역할이름HCID투입량
반응물Pivaloyl chlorideHCID 62493—
반응물Lithium ChlorideHCID 433294—
반응물4-Methyl-5-phenyl-2-oxazolidinone, (4S,5R)-HCID 853161—
반응물3-(2,4-difluorophenyl)propanoic AcidHCID 4986395—
용매TetrahydrofuranHCID 8028—
용매TriethylamineHCID 8471—
생성물(4R,5S)-3-[3-(2,4-Difluoro-phenyl)-propionyl]-4-methyl-5-phenyl-oxazolidin-2-oneHCID 6926711099%

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07179934B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-dd064df9909948a089c4e4418d5126f0
출처 메모uspto-grants-2007_02