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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644525Generated: October 30, 2026

Potassium Carbonate → 5-Cyano-7-(4-hydroxymethylphenyl)-1-phenylbenzimidazole

https://huagongshe.com/reaction/644525

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Hydroxymethyl)benzeneboronic acidHCID 2734706—
Reactant5-Cyano-7-(3-hydroxymethylphenyl)-1-phenylbenzimidazoleHCID 11393198—
Reactant5-Cyano-7-iodo-1-phenylbenzimidazoleHCID 67485627—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
Product5-Cyano-7-(4-hydroxymethylphenyl)-1-phenylbenzimidazoleHCID 67485006—

Reaction Steps

5-Cyano-7-(4-hydroxymethylphenyl)-1-phenylbenzimidazole was prepared from 5-cyano-7-iodo-1-phenylbenzimidazole (1.0 g, 2.90 mmol), 4-hydroxymethylphenylboronic acid (440 mg, 2.90 mmol), tetrakis(triphenylphosphine)palladium(0) (330 mg, 2.90 mmol) and potassium carbonate (2M in water, 2.9 ml, 800 mg, 5.8 mmol) in toluene (8.0 ml) and ethanol (2.0 ml) using the method described for 5-cyano-7-(3-hydroxymethylphenyl)-1-phenylbenzimidazole. 5-Cyano-7-(4-hydroxymethylphenyl)-1-phenylbenzimidazole was obtained as a white solid (711 mg) m/z, 326.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700638B2
Source datasetuspto-grants-2010_04
ORD IDord-3ac02db958504ecb8d09ec5b60bffbc2
Source noteuspto-grants-2010_04