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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922661Generated: November 2, 2026

Potassium Hydroxide → HCID 70983740, compound

https://huagongshe.com/reaction/922661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant4,5-DichloroimidazoleHCID 140018—
Reactant2-(Chloromethyl)quinoline hydrochlorideHCID 3083823—
SolventAcetonitrileHCID 6342—
ProductHCID 70983740HCID 70983740—

Reaction Steps

4,5-Dichloroimidazole (2.00 g, 14.6 mmol) was dissolved in 15 mL acetonitrile in a round bottom flask. Potassium hydroxide (0.90 g, 16.0 mmol) was added and the mixture was refluxed for 15 min. Concurrently, 2-chloromethylquinoline hydrochloride (3.13 g, 14.6 mmol) and potassium hydroxide (0.82 g, 14.6 mmol) were added to a second round bottom flask and stirred in 60 mL acetonitrile at reflux for 10 min. The contents of the second flask were added to the first, and the combined mixture was refluxed overnight, during which time a white precipitate formed. The reaction mixture was filtered hot, yielding a clear, tan filtrate. Slow evaporation and cooling of the filtrate yielded tan crystals of 1-(quinolin-2-ylmethyl)-4,5-dichloroimidazole, which were collected by a second filtration. The crystals (0.278 g, 1.0 mmol) will be dissolved in a minimum volume of DMF. Iodomethane (0.62 mL, 10.0 mmol) will be added and the mixture will be heated at 80° C. for 12 h. Removal of the volatile components under reduced pressure will yield the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278951B2
Source datasetuspto-grants-2016_03
ORD IDord-7754da2f5eaf43a380009b47d0cba06c
Source noteuspto-grants-2016_03