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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 635641생성일: 2026년 10월 24일

Sodium hydride → Diethyl 2-(tert-butoxyformamido)-2-[(5-oxazolyl)methyl]malonate

https://huagongshe.com/ko/reaction/635641

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물Diethyl 2-((tert-butoxycarbonyl)amino)malonateHCID 382219—
반응물5-(Chloromethyl)-1,3-oxazoleHCID 15290880—
용매EthanolHCID 702—
생성물Diethyl 2-(tert-butoxyformamido)-2-[(5-oxazolyl)methyl]malonateHCID 70092767—

반응 조건

온도0 °C

반응 단계

301 mg of a 60% dispersion of sodium hydride in mineral oil were added portionwise to 60 ml of anhydrous ethanol at 0° C. and the resulting suspension was stirred at 0° C. for 5 minutes. 1.88 g of diethyl 2-(tert-butoxyformamido)malonate were added and the mixture was warmed to room temperature. After stirring at room temperature for 10 minutes 805 mg of 5-(chloromethyl)oxazole were added. The mixture was stirred at room temperature for 30 minutes and at 60° C. for 1 hour. The solvent was evaporated and the crude product was dissolved in diethyl ether and washed with water. Sodium chloride was added to the aqueous layer, which was then extracted with diethyl ether. The combined organic layers were dried over magnesium sulphate and the solvent was removed by evaporation. Purification of the residue by chromatography on silica gel using ethyl acetate/hexane (1:2) for the elution gave diethyl 2-(tert-butoxyformamido)-2-[(5-oxazolyl)methyl]malonate, 1H NMR (250 MHz, CDCl3) δ: 1.3 (t,6H), 1.45 (s,9H), 3.75 (s,2H), 4.2 (m,4H), 5.85 (s,1H), 6.8 (s,1H), 7.75 (s,1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06187905B1
출처 데이터셋uspto-grants-2001_02
ORD IDord-f05699401b8847e68994ecec9e2d6bc7
출처 메모uspto-grants-2001_02