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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922594Generated: October 25, 2026

Potassium Hydroxide → 4,5-dichloro-1-(naphthalen-2-ylmethyl)-1H-imidazole

https://huagongshe.com/reaction/922594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant2-BromomethylnaphthaleneHCID 70320—
Reactant4,5-DichloroimidazoleHCID 140018—
SolventAcetonitrileHCID 6342—
Product4,5-dichloro-1-(naphthalen-2-ylmethyl)-1H-imidazoleHCID 7098209489.6%

Reaction Conditions

Temperature85 °C

Reaction Steps

4,5-dichloroimidazole (40.0 mmol, 5.479 g) and KOH (44.0 mmol, 2.469 g) were placed in a round bottom flask with 100 mL acetonitrile. The mixture was brought to reflux (85° C.) and stirred 1 h until KOH was consumed. 2-Bromomethylnapthalene (40.00 mmol, 8.844 g) was added and the solution was stirred at reflux for 17 hours. KBr was removed by vacuum filtration and the filtrate was collected. The volatiles were removed by rotary evaporation to give 4,5-dichloro-1-(naphthalen-2-ylmethyl)-1H-imidazole as a light brown solid. 4,5-dichloro-1-(naphthalen-2-ylmethyl)-1H-imidazole (18 mmol) was dissolved in acetonitrile (40 mL) in a round bottom flask. The solution was brought to reflux and iodomethane (5 mL) was added. The reaction was stirred at reflux for 20 h after which time it was cooled. The resulting white precipitate was collected by filtration and analyzed. Yield: 89.6% 1H NMR (300 MHz, d6-DMSO): δ 3.86 (s), 5.68 (s), 7.53-7.59 (m), 7.93-8.03 (m), 9.51 (s) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278951B2
Source datasetuspto-grants-2016_03
ORD IDord-f4a26f1b38d04f7bbabe98c68d2c87b7
Source noteuspto-grants-2016_03