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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441203Generated: November 2, 2026

Imidazole → 1,3-bis((1H-imidazol-1-yl)methyl)benzene

https://huagongshe.com/reaction/1441203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantPotassium HydroxideHCID 14797—
ReactantBenzene, 1,3-bis(bromomethyl)-HCID 69373—
SolventAcetoneHCID 180—
Product1,3-bis((1H-imidazol-1-yl)methyl)benzeneHCID 1122870163.9%

Reaction Steps

To a 500 mL round bottom flask equipped with a stirbar was added 11.6 g imidazole (170 mmol) and 9.55 g (170 mmol) finely pulverized potassium hydroxide. These were stirred in 200 mL acetone until the solution became yellow translucent. 15.0 g (56.8 mmol) α,α′-dibromo-m-xylene was then added, and the solution was stirred at room temperature overnight. The cloudy solution was filtered, and the white solids rinsed with acetone. The resulting filtrate was dried on silica and partitioned on a silica gel column using 30/70 acetonitrile/methanol as eluent. The product fractions were evaporated of solvent and the resulting oil recrystallized from ethyl acetate/hexanes to give 8.65 g 1-[3-(1H-imidazole-1yl-methyl)benzyl]-1H-imidazole as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07655322B2
Source datasetuspto-grants-2010_02
ORD IDord-c080b0cb6fe949c8a7c8a5bbb2ee371b
Source noteuspto-grants-2010_02