Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 5-Fluorouracil | HCID 3385 | — |
| Reactant | p-Anisoyl chloride | HCID 7477 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 15396960 | HCID 15396960 | 49.2% |
Reaction Steps
1.3 g (0.01 mole) of 5-fluorouracil was suspended in a mixed solution of 40 ml. of dioxane and 2 ml. of pyridine. 1.7 g (0.01 mole) of p-methoxybenzoyl chloride in 5 ml. of dioxane was added to the suspension and stirred at 80°C. for 5 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 ethanol and filtered. After cooling to 0°C., the resulting crystals were filtered and dried to give 1.30 g (49.2% yield) of 5-fluoro-1-(p-methoxybenzoyl)uracil. The product was recrystallized from dioxane-ethanol and white needles melting at 200°-201°C. were obtained. 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 |
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| Patent number | US03971784 |
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| Source dataset | uspto-grants-1976_07 |
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| ORD ID | ord-d5c2d220aa3c4e59a42e2c0387fe82e5 |
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| Source note | uspto-grants-1976_07 |
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