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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389057Generated: October 25, 2026

Bifonazole → 1,3-Bis-[alpha-(-biphenylyl)-benzyl]-imidazolium chloride

https://huagongshe.com/reaction/1389057

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBifonazoleHCID 2378—
Reactantalpha-Biphenylyl-benzyl chlorideHCID 13823625—
SolventAcetonitrileHCID 6342—
Product1,3-Bis-[alpha-(-biphenylyl)-benzyl]-imidazolium chlorideHCID 20298200122.2%

Reaction Steps

31 g (0.1 mol) of 1-[α-(4-biphenylyl)-benzyl]-imidazole and 27.9 g (0.1 mol) of α-biphenylyl-benzyl chloride are suspended in 200 ml of acetonitrile. The mixture is heated under reflux for 18 hours. The reaction mixture is then concentrated by distilling off the solvent and the residue, in 500 ml of toluene, is heated under reflux. The gel thereby formed is separated off and caused to crystallise by trituration with diisopropyl ether. 36 g (62% of theory) of 1,3-bis-[α-(-biphenylyl)-benzyl]-imidazolium chloride of melting point 150° C. (with decomposition) are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04243670
Source datasetuspto-grants-1981_01
ORD IDord-b2e8f8b42a1d4840979c37d9bd326313
Source noteuspto-grants-1981_01