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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918394Generated: October 31, 2026

5-Fluorouracil → 1-Benzenesulfonyl-5-fluorouracil

https://huagongshe.com/reaction/918394

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-FluorouracilHCID 3385—
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-DioxaneHCID 31275—
SolventEthanolHCID 702—
Product1-Benzenesulfonyl-5-fluorouracilHCID 55562254.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

2.6 g (0.02 mole) of 5-fluorouracil and 1.38 g (0.01 mole) of anhydrous potassium carbonate were suspended in 70 ml. of dioxane. 3.5 g (0.02 mole) of benzenesulfonyl chloride in 10 ml. of dioxane was dropwise added thereto and stirred at 80°C. for 7 hours. The reaction mixture was cooled to room temperature and filtered. The filtrate was concentrated under reduced pressure and a resinous residue was obtained. The residue was dissolved in a small amount of ethanol and allowed to stand at 5°C. overnight. There was obtained 2.95 g (54.6% yield) of 1-benzenesulfonyl-5-fluorouracil. The product was recrystallized from dioxane-ethanol and gave granular crystals melting at 256°-257°C. The results of an elementary analysis thereof were well in agreement with the calculated value as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03971784
Source datasetuspto-grants-1976_07
ORD IDord-0596ea97426749fd835c855fd11e614c
Source noteuspto-grants-1976_07