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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855878Generated: October 31, 2026

Imidazole → Dechloroclotrimazole

https://huagongshe.com/reaction/1855878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantTriphenylcarbinolHCID 6457—
ReactantDiphenoxyphosphanolateHCID 23418553—
SolventPyridineHCID 1049—
ProductDechloroclotrimazoleHCID 61823182.6%

Reaction Steps

A mixture of pyridine (15 ml), diphenyl phosphite (2.34 g, 10 mmole), imidazole (0.68 g, 10 mmole) and triphenylmethanol (2.08 g, 8 mmole) was refluxed for 3 hours. Pyridine was removed under reduced pressure, and the residue was extracted with dichloromethane. The extract was washed with a 5% aqueous hydroxide solution and water in order, dried and evaporated. Recrystallization of the residue (2.23 g) from acetonitrile gave 2.05 g of 1-triphenylmethylimidazole as colorless needles. Yield, 82.7%. M.P., 221°-223° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04216333
Source datasetuspto-grants-1980_08
ORD IDord-c2fa6fb78e2e44fd863e8a1b7810b6b6
Source noteuspto-grants-1980_08