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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189500Generated: October 26, 2026

Sodium Bicarbonate → 4-methoxy-2-[1-(4-trifluoromethoxyphenyl)-1H-imidazol-4-yl]-benzaldehyde

https://huagongshe.com/reaction/1189500

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant5-Methoxy-2-formylphenylboronic acidHCID 2734366—
ReactantWater 1,2-dimethoxyethaneHCID 18180031—
Reactant4-bromo-1-(4-(trifluoromethoxy)phenyl)-1H-imidazoleHCID 57824435—
CatalystHCID 178418476HCID 178418476—
SolventCyclohexaneHCID 8078—
SolventEthyl AcetateHCID 8857—
Product4-methoxy-2-[1-(4-trifluoromethoxyphenyl)-1H-imidazol-4-yl]-benzaldehydeHCID 5782441572.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

4-Bromo-1-(4-trifluoromethoxyphenyl)-1H-imidazole (100 mg, 0.326 mmol), 2-formyl-5-methoxyphenylboronic acid (73 mg, 0.41 mmol), bis(triphenylphosphine)palladium dichloride (2 mg, 0.003 mmol), sodium bicarbonate (49 mg, 0.59 mmol) and 1:1 DME/H2O (8:8 mL) were combined and added to a microwave vessel. The reaction mixture was heated in the microwave with stirring at 100° C. for 12 min. The microwave took 5 min to reach 100° C., then maintained at 100° C. for 12 min, and then cooled. TLC (1:1 EtOAc:cyclohexane) showed the presence of starting materials, thus the sample was heated to 100° C. for another 8 min. Upon cooling a precipitate formed; this was filtered and washed with water to give a grey solid (86 mg): ESIMS m/z 363.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674109B2
Source datasetuspto-grants-2014_03
ORD IDord-911641b6254d488ca68d32ae50828d58
Source noteuspto-grants-2014_03