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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2257946Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/2257946

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl bromoacetateHCID 7748—
Edukt5-Nitro-1-methoxymethyluracilHCID 18172488—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelTetrabutylammonium FluorideHCID 2724141—
ProduktEthyl 3,6-dihydro-3-(methoxymethyl)-5-nitro-2,6-dioxo-1(2H)-pyrimidineacetateHCID 21355699—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05658930
Quelldatensatzuspto-grants-1997_08
ORD IDord-cd36d30f556b41039d3eb352ab8ab3d7
Quellennotizuspto-grants-1997_08