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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085143Generated: October 26, 2026

Ethanol → 4-(2-Methyl-1H-imidazo[4,5-C]pyridin-1-YL)benzoic acid

https://huagongshe.com/reaction/1085143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
Reactant4-(2-Methyl-1H-imidazo[4,5-c]pyridin-1-yl)benzonitrileHCID 10681187—
Product4-(2-Methyl-1H-imidazo[4,5-C]pyridin-1-YL)benzoic acidHCID 10467437—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 4-(2-methylimidazo[4,5-c]pyrid-1-yl)benzonitrile (12.0 g, 51.3 mmol) and 40% aqueous sodium hydroxide (55 ml) in absolute ethanol (55 ml) was heated at reflux for 11/2 hours. The solvent was removed under reduced pressure, and the brown residue was dissolved in water. The solution was chilled to 0° C. by the addition of ice. Glacial acetic acid (ca 33 ml) was added slowly. The buff solid which precipitated was filtered off, washed with water, and dried in vacuo at 70° C. Yield 9.14 g (70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05008263
Source datasetuspto-grants-1991_04
ORD IDord-35d0f6e38701427a9e404141a1f6165c
Source noteuspto-grants-1991_04