HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643354Generated: November 4, 2026
Urea → 5-(1-Methylethyl)-2,4,6(1H,3H,5H)-pyrimidinetrione
https://huagongshe.com/reaction/1643354
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Urea | HCID 1176 | — |
| Reactant | 2-Bromopropane | HCID 6358 | — |
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-(1-Methylethyl)-2,4,6(1H,3H,5H)-pyrimidinetrione | HCID 81874 | 43.4% |
Reaction Steps
Sodium metal (1.28 kg, 55.65 mol) was dissolved in ethanol (25 L) under nitrogen atmosphere at 0° C. (bath temperature). Diethyl malonate (7.45 kg, 46.51 mol) was added to the solution and the mixture was heated to 80° C. 2-Bromopropane (8.00 kg, 65 mol) was added dropwise to the solution for 1 hour, and the solution was refluxed for 10 hours. The solution was cooled to room temperature. Sodium metal (1.22 kg, 53.04 mol) was dissolved into the solution under nitrogen atmosphere at 0° C. Urea (2.78 kg, 46.28 mol) in methanol (15 L) was added to the solution over 2 hours and the reaction mixture was refluxed for 20 hours. The reaction mixture was diluted with water (35 L) and conc. HCl (5 L), and cooled to room temperature. The precipitate was collected by filtration, washed with water (20 L), ether (15 L), n-hexane (20 L) and dried in vacuum at 40° C. for 10 hours to give 5-isopropylbarbituric acid as a white solid (3.42 kg, 20.10 mol, 43% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08119800B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-c6053edb77fd44cabe31e4607f917f38 |
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| Source note | uspto-grants-2012_02 |
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