HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393683Generated: October 26, 2026
Urea → 4-(3,5-Bis-trifluoromethylphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylic acid amide
https://huagongshe.com/reaction/393683
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Urea | HCID 1176 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Acetoacetamide | HCID 80077 | — |
| Reactant | 3,5-Bis(trifluoromethyl)benzaldehyde | HCID 136247 | — |
| Catalyst | Cupric Chloride | HCID 24014 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(3,5-Bis-trifluoromethylphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylic acid amide | HCID 86586005 | 36.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06809102B2 |
|---|
| Source dataset | uspto-grants-2004_10 |
|---|
| ORD ID | ord-b6dad4d14dd3474a9e23c7ce406e1919 |
|---|
| Source note | uspto-grants-2004_10 |
|---|