Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261975Generated: October 25, 2026

Potassium Iodide → 1-Benzyl-alpha,alpha-bis(p-chlorophenyl)imidazole-2-methanol

https://huagongshe.com/reaction/261975

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPicric AcidHCID 6954—
ReactantBenzyl BromideHCID 7498—
ReactantSodiumHCID 5360545—
ReactantBis-(4-chloro-phenyl)-(1H-imidazol-2-yl)-methanolHCID 12433870—
SolventAcetonitrileHCID 6342—
Product1-Benzyl-alpha,alpha-bis(p-chlorophenyl)imidazole-2-methanolHCID 12433938—

Reaction Steps

A solution of 19.2 g of α,α-bis(p-chlorophenyl)imidazole-2-methanol (prepared according to Example III B) and 3 g of sodium hydroxyde in 250 ml. of acetonitrile was refluxed for one hour with stirring. Then 500 mg of picric acid, a few crystals of potassium iodide and a solution of 11.3 g of benzyl bromide in 100 ml. of acetonitrile were added. Refluxing was then continued for 4 hours with stirring. The reaction mixture was kept standing overnight. The precipitate formed was filtered off and dissolved in 3 liter of diethyl ether. This solution was washed with a saturated sodium chloride solution, decolorized with active charcoal, dried over sodium sulphate and concentrated. The residue was crystallised from a mixture of methanol and diethyl ether. 1-Benzyl-α,α-bis(p-chlorophenyl)imidazole-2-methanol was obtained. Melting point 167°-168° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04152441
Source datasetuspto-grants-1979_05
ORD IDord-81c13b075a9449d79becd3cecb290bc5
Source noteuspto-grants-1979_05