Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918393Generated: November 1, 2026

5-Fluorouracil → 1-Methanesulfonyl-5-fluorouracil

https://huagongshe.com/reaction/918393

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-FluorouracilHCID 3385—
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-DioxaneHCID 31275—
ReactantMethanesulfonyl chlorideHCID 31297—
SolventMethanolHCID 887—
Product1-Methanesulfonyl-5-fluorouracilHCID 58275545.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

2.6 g. (0.02 mole) of 5-fluorouracil and 1.52 g (0.011 mole) of anhydrous potassium carbonate were suspended in 50 ml. of dioxane and then 2.53 g (0.022 mole) of methanesulfonyl chloride in 20 ml. of dioxane was dropwise added thereto. After stirring at 80°C. for 10 hours, the reaction mixture was filtered. The filtrate was concentrated under reduced pressure and a resinous residue was obtained. The residue was dissolved in a small amount of methanol and allowed to stand at 0°C. overnight. There was obtained 1.48 g (45.4% yield) of 5-fluoro-1 -methanesulfonyluracil. Recrystallization of the product from methanol gave leaflets melting at 223°-224°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-d30c5a64fb5c4515a760cc4923b5b9c1
Source noteuspto-grants-1976_07