HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215059Generated: October 27, 2026
Sodium Bicarbonate → ethyl 2-(2,4-dichlorophenyl)-5-methyl-1-(4-(trifluoromethyl)phenyl)-1H-imidazole-4-carboxylate
https://huagongshe.com/reaction/2215059
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Ethyl 3-bromo-2-oxobutanoate | HCID 11117285 | — |
| Reactant | HCID 178512013 | HCID 178512013 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | ethyl 2-(2,4-dichlorophenyl)-5-methyl-1-(4-(trifluoromethyl)phenyl)-1H-imidazole-4-carboxylate | HCID 11201587 | 52.4% |
Reaction Steps
Part C: 2,4-Dichloro-N-(4-(trifluoromethyl)phenyl)benzenecarboxamidine (15.0 g, 0.0450 mol) is dissolved in 2-propanol and ethyl 3-bromo-2-oxobutanoate (20.8 g, 2 molar equivalent) and NaHCO3 are successively added. The resulting mixture is heated at reflux temperature for 40 hours and allowed to attain room temperature. The 2-propanol is removed in vacuo, ethyl acetate is added to the residue and the resulting organic layer is washed with NaHCO3 (5% aqueous solution). The ethylacetate layer is collected, dried over Na2SO4, filtered and concentrated in vacuo. The resulting oil is purified by column chromatography (diethyl ether/petroleum ether=1/3 (v/v), silicagel) and further purified by crystallisation from cyclohexane to give ethyl 2-(2,4-dichlorophenyl)-5-methyl-1-(4-(trifluoromethyl)phenyl)-1H-imidazole-4-carboxylate (10.45 g, 52% yield) as a yellow solid. Melting point: 160–162° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07109216B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-58c26c34d65c4df3bd3b9c7b2ac97887 |
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| Source note | uspto-grants-2006_09 |
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