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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424861Generated: October 27, 2026

Hydrochloric Acid → 5-ethoxycarbonyl-4-(2-ethoxy-6-pentadecylphenyl)-6-methyl-3,4-dihydropyrimidin-2(1H)-one

https://huagongshe.com/reaction/424861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantUreaHCID 1176—
ReactantEthyl AcetoacetateHCID 8868—
Reactant2-Ethoxy-6-pentadecyl benzaldehydeHCID 22574570—
SolventTetrahydrofuranHCID 8028—
Product5-ethoxycarbonyl-4-(2-ethoxy-6-pentadecylphenyl)-6-methyl-3,4-dihydropyrimidin-2(1H)-oneHCID 10436532—

Reaction Steps

A solution of ethylacetoacetate (1.25 g, 8.5 mmol), 2-ethoxy-6-pentadecyl benzaldehyde (3 g, 8.5 mmol) and urea (1.1 g, 17 mmol) in tetrahydrofuran (20 mL) was heated to reflux (65-70° C.) in the presence of hydrochloric acid (30%) for 7 h. The reaction mixture after being cooled to room temperature was poured into crushed ice (20 g) and stirred for 5 min. The viscous liquid was extracted with ethylacetate (40 mL) and was washed with 1N hydrochloric acid, water, sodium bicarbonate and brine. After drying over anhydrous sodium sulfate, the solvent was evaporated to yield light yellow oil. This crude product was purified by flash column chromatography and recrystallized from hexane to get white crystalline solid of title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106062B1
Source datasetuspto-grants-2012_01
ORD IDord-9050021978d944ab8e7b8852d53edba8
Source noteuspto-grants-2012_01