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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922665Generated: October 30, 2026

Potassium Hydroxide → 1,3-Bis(quinoxalin-2-ylmethyl)-4,5-dichloroimidazolium bromide

https://huagongshe.com/reaction/922665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant4,5-DichloroimidazoleHCID 140018—
Reactant2-(Bromomethyl)quinoxalineHCID 5287759—
SolventAcetonitrileHCID 6342—
Product1,3-Bis(quinoxalin-2-ylmethyl)-4,5-dichloroimidazolium bromideHCID 86719694—

Reaction Steps

4,5-dichloroimidazole (1.37 g, 10 mmol) will be dissolved in a minimum amount of acetonitrile and potassium hydroxide (0.62 g, 11 mmol) will be added. The mixture will be stirred at reflux until the potassium hydroxide is consumed, approximately 30 min. 2-(Bromomethyl)quinoxaline (2.23 g, 10.0 mmol) will be added and the mixture will be returned to reflux for 3 h. The mixture will be filtered hot to remove the potassium bromide generated. A second addition of 2-(bromomethyl)quinoxaline (2.23 g, 10.0 mmol) will be made to the reaction solution, which will be returned to reflux for 6 h. Removal of the volatile components under reduced pressure should yield the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278951B2
Source datasetuspto-grants-2016_03
ORD IDord-054b5819a5b84d47a6bd73a2811a041e
Source noteuspto-grants-2016_03