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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 261975Erstellt: 27. Oktober 2026

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

https://huagongshe.com/reaction/261975

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium IodideHCID 4875—
EduktPicric AcidHCID 6954—
EduktBenzyl BromideHCID 7498—
EduktSodiumHCID 5360545—
EduktBis-(4-chloro-phenyl)-(1H-imidazol-2-yl)-methanolHCID 12433870—
LösungsmittelAcetonitrileHCID 6342—
Produkt1-Benzyl-alpha,alpha-bis(p-chlorophenyl)imidazole-2-methanolHCID 12433938—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04152441
Quelldatensatzuspto-grants-1979_05
ORD IDord-81c13b075a9449d79becd3cecb290bc5
Quellennotizuspto-grants-1979_05