HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918394Generated: October 31, 2026
5-Fluorouracil → 1-Benzenesulfonyl-5-fluorouracil
https://huagongshe.com/reaction/918394
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Fluorouracil | HCID 3385 | — |
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Benzenesulfonyl-5-fluorouracil | HCID 555622 | 54.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US03971784 |
|---|
| Source dataset | uspto-grants-1976_07 |
|---|
| ORD ID | ord-0596ea97426749fd835c855fd11e614c |
|---|
| Source note | uspto-grants-1976_07 |
|---|