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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922667Generated: October 31, 2026

Acetonitrile → HCID 86719698, compound

https://huagongshe.com/reaction/922667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPotassium HydroxideHCID 14797—
Reactant4,5-DichloroimidazoleHCID 140018—
Reactant2-(Bromomethyl)anthraceneHCID 19012961—
ProductHCID 86719698HCID 86719698—

Reaction Steps

4,5-Dichloroimidazole (0.18 g, 1.33 mmol) and potassium hydroxide (0.08 g, 1.46 mmol) will be dissolved in a minimum volume of acetonitrile and stirred at reflux for 30 min. 2-(Bromomethyl)anthracene (2.71 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 KBr generated. A solution of 2-(chloromethyl)quinoline will be prepared by combining 2-(chloromethyl)quinolone hydrochloride (2.14 g, 10 mmol) and potassium hydroxide (0.56 g, 10.0 mmol) in acetonitrile and refluxing the mixture for 30 min, and this solution will be added to the filtrate. The combined mixture will be returned to reflux for 6 h. The volatile components will be removed under reduced pressure, and the resulting solid will be washed with water to remove the KCl generated in the neutralization of the quinoline. The remaining solid will be dried and will be the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278951B2
Source datasetuspto-grants-2016_03
ORD IDord-24e7e9f1597b4a7e8a341ebac347d5b2
Source noteuspto-grants-2016_03