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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475669Generated: October 29, 2026

Potassium Carbonate → 4'-(4-Bromo-2-ethoxy-5-formylimidazol-1-ylmethyl)-3'-fluorobiphenyl-2-carboxylic acid t-butyl ester

https://huagongshe.com/reaction/475669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTert-butyl 4'-bromomethyl-3'-fluoro-biphenyl-2-carboxylateHCID 53375348—
ReactantHCID 178467395HCID 178467395—
SolventDimethylformamideHCID 6228—
Product4'-(4-Bromo-2-ethoxy-5-formylimidazol-1-ylmethyl)-3'-fluorobiphenyl-2-carboxylic acid t-butyl esterHCID 5104157215.7%

Reaction Steps

5-Bromo-2-ethoxy-3H-imidazole-4-carbaldehyde (10.0 g, 45.6 mmol), 4′-bromomethyl-3′-fluorobiphenyl-2-carboxylic acid t-butyl ester (16.7 g, 45.6 mmol) and potassium carbonate (9.5 g, 68.5 mmol) were dissolved in DMF (200 mL) at 0° C. After 10 minutes, the mixture was allowed to warm to room temperature and was stirred overnight. The mixture was filtered and concentrated in vacuo. The concentrate was extracted with EtOAc (2×200 mL) and sat. aq. NaHCO3:water; 1:1 (150 mL). The combined organic fractions were dried over Na2SO4, filtered, and concentrated in vacuo. The crude material was recrystallized from EtOH (20 mL) and water (40 mL) to afford a white solid. The filtrate was concentrated in vacuo and purified by silica gel chromatography (EtOAc:hexanes) to yield the title compound as a white solid (3.6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637562B2
Source datasetuspto-grants-2014_01
ORD IDord-aecf4fa7fb904ea1a419fed82ee0a148
Source noteuspto-grants-2014_01