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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49150생성일: 2026년 10월 24일

Hydrochloric Acid → 5-(2-Ethoxy-ethyl)-pyrimidine-2,4,6-trione

https://huagongshe.com/ko/reaction/49150

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물UreaHCID 1176—
반응물Diethyl MalonateHCID 7761—
반응물2-Bromoethyl ethyl etherHCID 61141—
반응물SodiumHCID 5360545—
용매EthanolHCID 702—
생성물5-(2-Ethoxy-ethyl)-pyrimidine-2,4,6-trioneHCID 21931023—

반응 단계

Sodium metal (8.6 g, 0.38 mol) was added to ethanol (375 mL), and the mixture was stirred at ambient temperature until homogeneous. Diethyl malonate (60 g, 0.38 mol) was added, followed by bromoethyl ethyl ether (57.4 g, 0.38 mol). After stirring at reflux for 3 hours, the mixture was cooled to ambient temperature and concentrated in vacuo. The resulting material was added to a mixture of sodium ethoxide and ethanol (prepared by the reaction of 17.2 g of sodium metal with 600 mL of methanol). Urea (24 g) was added, and the resulting mixture was refluxed for 2.5 hours. After cooling to ambient temperature, the mixture was stirred for 12 hours, acidified with 1M hydrochloric acid solution, extracted three times with ethyl acetate, and the combined organic layers were dried over sodium sulfate (Na2SO4), filtered and concentrated in vacuo, affording 5-(2-ethoxy-ethyl)-pyrimidine-2,4,6-trione as a colorless solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06706723B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-c231ce5deda648a49df05045f30d520a
출처 메모uspto-grants-2004_03