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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 397008생성일: 2026년 10월 24일

Ethyl bromoacetate → Ethyl 3,6-dihydro-3-(methoxymethyl)-5-nitro-2,6-dioxo-1(2H)-pyrimidineacetate

https://huagongshe.com/ko/reaction/397008

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl bromoacetateHCID 7748—
반응물5-Nitro-1-methoxymethyluracilHCID 18172488—
용매TetrahydrofuranHCID 8028—
용매Tetrabutylammonium FluorideHCID 2724141—
생성물Ethyl 3,6-dihydro-3-(methoxymethyl)-5-nitro-2,6-dioxo-1(2H)-pyrimidineacetateHCID 21355699—

반응 단계

The compound of example 41 (10.0 g, 50 mmole) is dissolved in tetrabutylammonium flouride (120 mL of a 1.0M solution in tetrahydrofuran, 0.124 mole). Ethyl bromoacetate (8.3 mL, 75 mmole) is added. The reaction is stirred at room temperature. The reaction mixture is concentrated, then partitioned between dichloromethane and water. The aqueous layer is extracted with dichloromethane. The combined organic extracts are washed with water, brine, and dried over anhydrous magnesium sulfate. The solvent is removed under vacuum to afford the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06608204B1
출처 데이터셋uspto-grants-2003_08
ORD IDord-96a36b6cadd045c68beeb6ee26e579cb
출처 메모uspto-grants-2003_08