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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1985384생성일: 2026년 10월 24일

Pivaloyl chloride → (4S)-4-benzyl-3-(2-isopropoxyacetyl)oxazolidin-2-one

https://huagongshe.com/ko/reaction/1985384

반응식

참여 물질

역할이름HCID투입량
반응물Pivaloyl chlorideHCID 62493—
반응물Lithium ChlorideHCID 433294—
반응물2-(Propan-2-yloxy)acetic acidHCID 517213—
반응물(S)-4-Benzyl-2-oxazolidinoneHCID 736225—
용매TetrahydrofuranHCID 8028—
용매TriethylamineHCID 8471—
생성물(4S)-4-benzyl-3-(2-isopropoxyacetyl)oxazolidin-2-oneHCID 5999795156.8%

반응 조건

온도-25 °C

반응 단계

A solution containing 98 g of 2-isopropoxyacetic acid and 360 ml of triethylamine in tetrahydrofuran (4L) was cooled to −25° C. After 92 ml of 2,2-dimethylpropanoyl chloride was dropwise added, the reaction solution was stirred at −20° C. for 5 hours. Then, 50 g of anhydrous lithium chloride and 120 g of (4S)-4-benzyl-1,3-oxazolidin-2-one were successively added, and stirring was continued at room temperature overnight. Then, the reaction solution was filtered and evaporated. The residue was dissolved in 2 L of ethyl acetate, washed with saturated aqueous sodium hydrogen carbonate, and then dried over anhydrous magnesium sulfate. The solvent was evaporated, and the residue was purified by silica gel column chromatography (elution solvent: hexane-ethyl acetate), to give 106.6 g of (4S)-4-benzyl-3-(2-isopropoxyacetyl)-1,3-oxazolidin-2-one as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07544835B2
출처 데이터셋uspto-grants-2009_06
ORD IDord-5178ef5a9d284d738f013980ea07e27d
출처 메모uspto-grants-2009_06