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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419123Generated: October 26, 2026

Benzyl Bromide → Methyl 1-benzyl-1H-benzimidazole-5-carboxylate

https://huagongshe.com/reaction/1419123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactantmethyl 1H-1,3-benzodiazole-5-carboxylateHCID 2779733—
SolventAcetoneHCID 180—
ProductMethyl 1-benzyl-1H-benzimidazole-5-carboxylateHCID 5445048822.2%

Reaction Steps

A mixture of 2.8 g of methyl 5-benzimidazolecarboxylate (prepared as described in Preparation 26), 3.52 g of benzyl bromide, 3 g of potassium carbonate and 50 ml of acetone was stirred for 3 days at room temperature. At the end of this time, the solvent was removed by evaporation under reduced pressure and the residue was mixed with an aqueous solution of sodium chloride, after which it was extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate, after which the solvent was removed by distillation under reduced pressure. The residue was then recrystallized from a mixture of ethyl acetate and hexane, to give 0.94 g of the title compound, melting at 156°-162° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05886014
Source datasetuspto-grants-1999_03
ORD IDord-ba3e220a895f48f4abeccf9969b9d70b
Source noteuspto-grants-1999_03