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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446706Generated: October 30, 2026

Benzyl Bromide → 3-Benzyl-1-methyl-4-phenylimidazolium bromide

https://huagongshe.com/reaction/446706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
Reactant1-methyl-4-phenyl-1H-imidazoleHCID 2748782—
SolventTolueneHCID 1140—
Product3-Benzyl-1-methyl-4-phenylimidazolium bromideHCID 8665518590%

Reaction Steps

In a 25 ml one-necked flask, there is dissolved 0.320 g (2.023 mmol) of 1-methyl-4-phenylimidazole, which was obtained according to P. Benjes et al., Heterocycles (1994), 37(2), 735-38, in 10 ml of toluene and then 0.36 ml (3.035 mmol) of benzyl bromide is added. After 5 days of heating under reflux, the reaction medium is concentrated under reduced pressure. The residue is taken up in 50 ml of diisopropyl ether. The precipitate formed is drained, washed twice with 5 ml of diisopropyl ether, and then dried under reduced pressure. 0.500 g (90%) of 3-benzyl-1-methyl-4-phenylimidazolium bromide is thus obtained in the form of a beige-grey solid whose characteristics are the following:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481522B2
Source datasetuspto-grants-2013_07
ORD IDord-59ac433b26974aa6a7dd57041b59ba32
Source noteuspto-grants-2013_07