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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1977234Generated: October 27, 2026

Water → 1-Benzyl-5-bromo-1,2,3,4-tetrahydropyrimidine-2,4-dione

https://huagongshe.com/reaction/1977234

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant5-BromouracilHCID 5802—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
SolventDimethylformamideHCID 6228—
Product1-Benzyl-5-bromo-1,2,3,4-tetrahydropyrimidine-2,4-dioneHCID 5276659—

Reaction Steps

To a suspension of 5-bromouracil (5.0 g, 26 mmol) and potassium carbonate (7.2 g, 52 mmol) in N,N-dimethylformamide (25 mL) was added benzyl bromide (3.1 mL, 26 mmol) and the reaction mixture stirred 72 h. The reaction was treated with water (50 mL) and then extracted into ethyl acetate (3×75 mL). The aqueous layer was further extracted with dichloromethane (3×100 mL), the dichloromethane layers were combined, washed with water (2×50 mL), brine (1×50 mL), dried over magnesium sulfate, filtered and concentrated in vacuo. The resulting mixture of products was purified by pressurized silica gel chromatography (25% ethyl acetate in hexane) to provide 1-benzyl-5-bromo-1H-pyrimidine-2,4-dione.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06232318B1
Source datasetuspto-grants-2001_05
ORD IDord-64473c567bd74c09b44d694d7fd48f7d
Source noteuspto-grants-2001_05