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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397008Generated: October 26, 2026

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

https://huagongshe.com/reaction/397008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
Reactant5-Nitro-1-methoxymethyluracilHCID 18172488—
SolventTetrahydrofuranHCID 8028—
SolventTetrabutylammonium FluorideHCID 2724141—
ProductEthyl 3,6-dihydro-3-(methoxymethyl)-5-nitro-2,6-dioxo-1(2H)-pyrimidineacetateHCID 21355699—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608204B1
Source datasetuspto-grants-2003_08
ORD IDord-96a36b6cadd045c68beeb6ee26e579cb
Source noteuspto-grants-2003_08