HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371913Generated: October 30, 2026
5-Fluorouracil → 3-Benzoyl-5-fluoropyrimidine-2,4(1H,3H)-dione
https://huagongshe.com/reaction/371913
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Fluorouracil | HCID 3385 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-Benzoyl-5-fluoropyrimidine-2,4(1H,3H)-dione | HCID 12690827 | 32% |
Reaction Steps
2.6 g (0.02 mole) of 5-fluorouracil was suspended in 10 ml of absolute pyridine and 10 ml of absolute dioxane, and the suspension was warmed to 80° C and stirred. 5.6 g (0.04 mole) of benzoyl chloride was then added dropwise thereto followed by stirring at 80° C for 1.5 hours to allow the mixture to react. After completion of the reaction, the reaction mixture was poured into ice-water followed by stirring, and the thus precipitated solid was filtered, washed with water and then dissolved in benzene while hot (80° C). Any insoluble matter was removed by filtration, and the filtrate allowed to cool to precipitate crystals, which were recovered by filtration to obtain 1.5 g of 3-N-benzoyl-5-fluorouracil in a yield of 32% (the filtrate was set aside). Melting Point: 170° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04088646 |
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| Source dataset | uspto-grants-1978_05 |
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| ORD ID | ord-9197ed243b7b4729b6952044f0c2c95e |
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| Source note | uspto-grants-1978_05 |
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