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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantUreaHCID 1176—
Reactant2-BromopropaneHCID 6358—
ReactantDiethyl MalonateHCID 7761—
ReactantSodiumHCID 5360545—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product5-(1-Methylethyl)-2,4,6(1H,3H,5H)-pyrimidinetrioneHCID 8187443.4%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119800B2
Source datasetuspto-grants-2012_02
ORD IDord-c6053edb77fd44cabe31e4607f917f38
Source noteuspto-grants-2012_02