HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918393Generated: November 1, 2026
5-Fluorouracil → 1-Methanesulfonyl-5-fluorouracil
https://huagongshe.com/reaction/918393
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Fluorouracil | HCID 3385 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Methanesulfonyl-5-fluorouracil | HCID 582755 | 45.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US03971784 |
|---|
| Source dataset | uspto-grants-1976_07 |
|---|
| ORD ID | ord-d30c5a64fb5c4515a760cc4923b5b9c1 |
|---|
| Source note | uspto-grants-1976_07 |
|---|