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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707662Generated: November 1, 2026

Hydrochloric Acid → 1H-Imidazole, 2-(2-benzofuranyl)-1-methyl-, monohydrochloride

https://huagongshe.com/reaction/1707662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant1H-Imidazole, 2-(2-benzofuranyl)-, monohydrochlorideHCID 3073595—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventDiethyl ether ethanolHCID 21585056—
Product1H-Imidazole, 2-(2-benzofuranyl)-1-methyl-, monohydrochlorideHCID 3073597—

Reaction Steps

To a solution of the free base (7.0 g) generated from 2-(benzofuran-2-yl)imidazole hydrochloride in DMF (50 ml) at 0° C. was added sodium hydride (1.4 g) 80% in mineral oil in three equal portions. After 30 minutes at room temperature, methyl iodide (2.5 ml) was added dropwise over 15 minutes at 0° C. The mixture was then stirred for 30 minutes at room temperature, poured into water and extracted with ethyl acetate. The organic layer was washed with water and the product was extracted with hydrochloric acid (1M). The aqueous layer was basified with sodium hydroxide and the free base was extracted with ethyl acetate, washed with saturated brine and dried. Evaporation of the solvent gave a solid residue which was dissolved in diethyl ether/ethanol. Ethereal HCl was added to solution and the precipitated salt was collected by filtration (8.1 g, 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05354769
Source datasetuspto-grants-1994_10
ORD IDord-19ec5445c00f4e16a0ee0c4a8f5a4475
Source noteuspto-grants-1994_10