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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 349823생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/349823

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
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—
생성물3-(2-Methyl-pent-2-enoyl)-4-phenyl-oxazolidin-2-oneHCID 6904824899%

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 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07179934B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-b24b07d8b7dc45fb9b56dd08ab118735
출처 메모uspto-grants-2007_02