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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678082Generated: November 1, 2026

Water → HCID 66737436, compound

https://huagongshe.com/reaction/1678082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Bromo-4-chlorobutaneHCID 81364—
ReactantHCID 178517770HCID 178517770—
SolventDimethyl SulfoxideHCID 679—
SolventDimethylformamideHCID 6228—
ProductHCID 66737436HCID 66737436—

Reaction Conditions

Temperature20 °C

Reaction Steps

2.6 g (15.0 mmol) of 1-bromo-4-chlorobutane were added dropwise to a solution of 1.95 g (15.0 mmol) of 2,4-dihydroxy-5-fluoropyrimidine in 50 ml of dimethyl sulfoxide and 20.0 ml of N,N-dimethylformamide (DMF) at 0° C. 2.07 g (15.0 mmol) of K2CO3 were added in portions over the course of 1 hour, and the mixture was stirred at 20° C. for 1 hour (dialkylated product is already identifiable). Water was then added to the reaction mixture, and the aqueous mixture was extracted twice with diethyl ether and twice with methylene chloride. The aqueous phase was adjusted to pH 3-4 with hydrochloric acid and then the aqueous phase was extracted with methylene chloride. The organic phase was then dried, the desiccant was removed by filtration, and the solvent was evaporated to dryness in vacuo; yield: 0.6 g. 1-(4-Chlorobutyl)-5-fluoropyrimidine-2,4(1H,3H)-dione was employed without further purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008488B2
Source datasetuspto-grants-2011_08
ORD IDord-59e10ce41e1d4458bb0697ae36126c78
Source noteuspto-grants-2011_08