HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49150Generated: October 25, 2026
Hydrochloric Acid → 5-(2-Ethoxy-ethyl)-pyrimidine-2,4,6-trione
https://huagongshe.com/reaction/49150
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Urea | HCID 1176 | — |
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | 2-Bromoethyl ethyl ether | HCID 61141 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-(2-Ethoxy-ethyl)-pyrimidine-2,4,6-trione | HCID 21931023 | — |
Reaction Steps
Sodium metal (8.6 g, 0.38 mol) was added to ethanol (375 mL), and the mixture was stirred at ambient temperature until homogeneous. Diethyl malonate (60 g, 0.38 mol) was added, followed by bromoethyl ethyl ether (57.4 g, 0.38 mol). After stirring at reflux for 3 hours, the mixture was cooled to ambient temperature and concentrated in vacuo. The resulting material was added to a mixture of sodium ethoxide and ethanol (prepared by the reaction of 17.2 g of sodium metal with 600 mL of methanol). Urea (24 g) was added, and the resulting mixture was refluxed for 2.5 hours. After cooling to ambient temperature, the mixture was stirred for 12 hours, acidified with 1M hydrochloric acid solution, extracted three times with ethyl acetate, and the combined organic layers were dried over sodium sulfate (Na2SO4), filtered and concentrated in vacuo, affording 5-(2-ethoxy-ethyl)-pyrimidine-2,4,6-trione as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06706723B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-c231ce5deda648a49df05045f30d520a |
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| Source note | uspto-grants-2004_03 |
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