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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1251344Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1251344

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 mixture 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
PatentnummerUS06342504B1
Quelldatensatzuspto-grants-2002_01
ORD IDord-3fd491269df0455f839f54dff31c2096
Quellennotizuspto-grants-2002_01