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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612800Generated: November 1, 2026

Hydrochloric Acid → 2-Butyl-1-(4-iodobenzyl)imidazol-4,5-dicarboxylic acid

https://huagongshe.com/reaction/612800

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactant4-Iodobenzyl bromideHCID 954258—
ReactantDimethyl 2-butyl-1H-imidazole-4,5-dicarboxylateHCID 14955796—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
Product2-Butyl-1-(4-iodobenzyl)imidazol-4,5-dicarboxylic acidHCID 1959641887.6%

Reaction Steps

Dimethyl 2-butylimidazol-4,5-dicarboxylic acid (7.12 g, 29.6 mmol) and 4-iodobenzyl bromide (10.56 g, 35.5 mmol) were dissolved in DMF (50 ml), and 60% oily sodium hydride (1.3 g, 32.5 mmol) was added in small portions while stirring at room temperature. The reaction solution was stirred at room temperature for 2 hours and methanol was added to treat excess sodium hydride. Then the reaction solution was neutralized with 2N HCl and the product was extracted with dichloromethane. The extracted solution was dried over sodium sulfate and concentrated in reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:1) to give the titled compound (11.1 g, 82%) as a tan solid (mp:98-99° C., Rf:0.60 silica gel-ethyl acetate/hexane/=1/1). This has the following NMR spectrum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06005105
Source datasetuspto-grants-1999_12
ORD IDord-cdf31f20f8224348856ae100cc0069cf
Source noteuspto-grants-1999_12