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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183553Generated: October 27, 2026

Urea → 4-(3,5-Bis-trifluoromethylphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylic acid amide

https://huagongshe.com/reaction/2183553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantUreaHCID 1176—
ReactantBoron trifluoride etherateHCID 8000—
ReactantAcetoacetamideHCID 80077—
Reactant3,5-Bis(trifluoromethyl)benzaldehydeHCID 136247—
CatalystCupric ChlorideHCID 24014—
SolventAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
Product4-(3,5-Bis-trifluoromethylphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylic acid amideHCID 8658600536.2%

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of 3,5-bis(trifluoromethyl)benzaldehyde (2.42 g, 10.0 mmol), acetoacetamide (1.01 g, 10.0 mmol), urea (0.90 g, 15.0 mmol), copper chloride (0.1 g, 1.0 mmol), boron trifluoride etherate (0.09 mL), AcOH (0.04 mL), and THF (20 mL) was heated at 65° C. for 18 h and cooled to room temperature. The resulting precipitates were collected by vacuum filtration, washed with THF, and air dried to give the title compound as an off-white solid (1.33 g, 36%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900214B2
Source datasetuspto-grants-2005_05
ORD IDord-56dcc4c1e5f845048640199c8dff261c
Source noteuspto-grants-2005_05