Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855869Generated: October 25, 2026

Imidazole → Clotrimazole

https://huagongshe.com/reaction/1855869

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactant(2-Chlorophenyl)diphenylmethanolHCID 298659—
ReactantDiphenoxyphosphanolateHCID 23418553—
SolventBenzeneHCID 241—
ProductClotrimazoleHCID 281272.8%

Reaction Steps

A mixture of benzene (20 ml), diphenyl phosphite (5.62 g, 24 mmole), imidazole (2.45 g, 36 mmole) and o-chlorophenyldiphenylmethanol (2.95 g, 10 mmole) obtained in Example 1 (A) was refluxed for 8 hours. After cooling, the reaction mixture was washed with a 5% aqueous potassium hydroxide solution (20 ml). The benzene layer was separated, washed with water, dried over magnesium sulfate and evaporated. Recrystallization of the crystalline residue from acetonitrile gave 2.51 g of 1-(o-chlorophenyldiphenylmethyl)imidazole. Yield, 73%. M.P., 142°-143° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04216333
Source datasetuspto-grants-1980_08
ORD IDord-a535584c4d384c0e9d7126cfb1f6c87a
Source noteuspto-grants-1980_08