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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795257Generated: November 2, 2026

Triphenylcarbinol → 2-(1-Trityl-1H-imidazol-4-yl)-benzonitrile

https://huagongshe.com/reaction/1795257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylcarbinolHCID 6457—
Reactant4-(2-bromophenyl)-1-trityl-1H-imidazoleHCID 22185143—
ReactantHCID 178418546HCID 178418546—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
Product2-(1-Trityl-1H-imidazol-4-yl)-benzonitrileHCID 22185159—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 4-(2-bromo-phenyl)-1-trityl-1H-imidazole (73.0 g, 163.3 mmol) in dimethylformamide (500 ml) was added copper (I) cyanide (17.5 g, 195.9 mmol). The reaction was heated to ˜80° C. under nitrogen for 14 h. After cooling to about 50° C., the reaction was diluted with toluene (ca. 300 ml) and slowly poured onto ammonium hydroxide (3N, 1.5 L) while stirring vigorously. The mixture was stirred for 40 min and then filtered in vacuo over a bed of celite (slow filtration, required ˜2 h). The phases were separated and the organic layer was washed with brine (75 ml×3) and dried (sodium sulfate). Concentration of the solvent afforded a light brown solid. The crude product contains ˜10–15% of trityl alcohol (by HPLC) and was used without further purification in the subsequent step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07026324B2
Source datasetuspto-grants-2006_04
ORD IDord-6268f68576ce443bb9613929eb45e039
Source noteuspto-grants-2006_04