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HRID 349816作成日:2026年10月27日

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

https://huagongshe.com/reaction/349816

反応式

関与物質

役割名称HCID仕込み量
反応物Pivaloyl chlorideHCID 62493—
反応物Lithium ChlorideHCID 433294—
反応物4-Methyl-5-phenyl-2-oxazolidinone, (4S,5R)-HCID 853161—
反応物3-(2,4-difluorophenyl)propanoic AcidHCID 4986395—
溶媒TetrahydrofuranHCID 8028—
溶媒TriethylamineHCID 8471—
生成物(4R,5S)-3-[3-(2,4-Difluoro-phenyl)-propionyl]-4-methyl-5-phenyl-oxazolidin-2-oneHCID 6926711099%

反応条件

温度0 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07179934B2
出典データセットuspto-grants-2007_02
ORD IDord-dd064df9909948a089c4e4418d5126f0
出典メモuspto-grants-2007_02