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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38306생성일: 2026년 10월 24일

Ethyl Acetate → 3-(2-Oxo-1,3-oxazolidin-3-yl)benzaldehyde

https://huagongshe.com/ko/reaction/38306

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물2-BromoethanolHCID 10898—
반응물Sodium hydrideHCID 24758—
반응물3-(BOC-Amino)benzaldehydeHCID 16740736—
용매DimethylformamideHCID 6228—
생성물3-(2-Oxo-1,3-oxazolidin-3-yl)benzaldehydeHCID 2313182429.6%

반응 단계

To a solution of 2.93 g of 3-[N-(t-butoxycarbonyl)amino]benzaldehyde in 20 ml of dimethylformamide was added 0.58 g of sodium hydride (60% oily) under ice-cooling. After stirring at room temperature for 1 hour, a solution of 0.93 ml of 2-bromoethanol in 5 ml of dimethylformamide was added dropwise under ice-cooling. After stirring at room temperature for 14 hours, the mixture was heated to stir at 115° C. for 6 hours. Ethyl acetate was added, and this was washed successively with water and an aqueous saturated sedum chloride solution, dried with anhydrous sodium sulfate, and concentrated. The residue was subjected to silica gel column chromatography to obtain 0.75 g of oily 3-(2-oxo-oxazolidin-3-yl)benzaldehyde.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524729B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-66c3dc5457934a1f8fca48a64bde6623
출처 메모uspto-grants-2013_09