HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Fluorouracil → 1-(p-Toluenesulfonyl)-5-fluorouracil
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Fluorouracil | HCID 3385 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-(p-Toluenesulfonyl)-5-fluorouracil | HCID 562851 | 62.3% |
Reaction Steps
2.6 g (0.02 mole) of 5-fluorouracil and 1.28 g (0.01 mole) of anhydrous potassium carbonate were suspended in 50 ml. of dioxane and reacted with 3.82 g (0.02 mole) of p-toluenesulfonyl chloride in the same manner as in Example 10. There was obtained 3.54 g (62.3% yield) of 5-fluoro-1-(p-toluenesulfonyl)uracil. Recrystallization of the product from methanol-chloroform gave leaflets melting at 241°-242°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-651ceeec4d04406abbf708e9fc98ed3c |
| Source note | uspto-grants-1976_07 |