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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Pivaloyl chloride | HCID 62493 | — |
| 반응물 | Lithium Chloride | HCID 433294 | — |
| 반응물 | 4-Methyl-5-phenyl-2-oxazolidinone, (4S,5R)- | HCID 853161 | — |
| 반응물 | 3-(2,4-difluorophenyl)propanoic Acid | HCID 4986395 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Triethylamine | HCID 8471 | — |
| 생성물 | (4R,5S)-3-[3-(2,4-Difluoro-phenyl)-propionyl]-4-methyl-5-phenyl-oxazolidin-2-one | HCID 69267110 | 99% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07179934B2 |
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| 출처 데이터셋 | uspto-grants-2007_02 |
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| ORD ID | ord-dd064df9909948a089c4e4418d5126f0 |
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| 출처 메모 | uspto-grants-2007_02 |
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