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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261971Generated: October 26, 2026

Potassium Iodide → HCID 21321305, compound

https://huagongshe.com/reaction/261971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantMethyl iodideHCID 6328—
ReactantPicric AcidHCID 6954—
ReactantSodium HydroxideHCID 14798—
ReactantBis-(4-chloro-phenyl)-(1H-imidazol-2-yl)-methanolHCID 12433870—
SolventAcetonitrileHCID 6342—
ProductHCID 21321305HCID 21321305—

Reaction Steps

To a suspension of 9.6 g (0.030 mol) of α,α-bis(p-chlorophenyl)imidazole-2-methanol (prepared according to Example III) in 100 ml. of acetonitrile, 500 mg of picric acid, 300 mg of potassium iodide and 1.45 g (0.036 mol) of sodium hydroxide were added at 60° C. The reaction mixture was stirred for one hour and then 4.7 g (0.033 mol) of methyl iodide in 25 ml. of acetonitrile were added dropwise at 55° C. The mixture was refluxed for four hours, the solvent was distilled off and the residue was extracted with a mixture of water and diethyl ether. The solid matter was filtered off and the ethereal phase was dried over sodium sulphate and concentrated. Diethyl ether was added to the residue and the solid matter was filtered off. The two portions of solid material were combined and twice crystallised from isopropyl alcohol and twice from toluene and rewashed with petroleum ether (boiling range 60°-80° C.). α,α-Bis(p-chlorophenyl)-1-methylimidazole-2-methanol was obtained. Melting point 190°-191° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04152441
Source datasetuspto-grants-1979_05
ORD IDord-fa1e8f200d2b431ba484ee83dd61595a
Source noteuspto-grants-1979_05