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HRID 132642作成日:2026年10月25日

Triethylamine → 3-(2-Methyl-pent-2-enoyl)-4-phenyl-oxazolidin-2-one

https://huagongshe.com/reaction/132642

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
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—
生成物3-(2-Methyl-pent-2-enoyl)-4-phenyl-oxazolidin-2-oneHCID 6904824899%

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 were 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US07388023B2
出典データセットuspto-grants-2008_06
ORD IDord-289944013d874fbd9224757487df27d7
出典メモuspto-grants-2008_06