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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 265157Generated: October 26, 2026

Trityl chloride → 2-Butyl-1-tritylimidazole-4,5-dicarbonitrile

https://huagongshe.com/reaction/265157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
Reactant2-butyl-1H-imidazole-4,5-dicarbonitrileHCID 5260591—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-Butyl-1-tritylimidazole-4,5-dicarbonitrileHCID 1903613882.2%

Reaction Steps

1.25 g of sodium hydride (as a 55% w/w dispersion in mineral oil) were added, whilst ice-cooling, to a solution of 5 g of 2-butylimidazole-4,5-dicarbonitrile (prepared as described in Preparation 1) in 50 ml of N,N-dimethylformamide, and the resulting mixture was stirred for 15 minutes. 10 g of trityl chloride were then added, and the reaction mixture was stirred at 50° C. for 6 hours. At the end of this time, it was mixed with ethyl acetate and water, and the product was extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate, and the solvent was removed by distillation under reduced pressure. The resulting residue was purified by column chromatography through silica gel, using a 1:5 by volume mixture of ethyl acetate and hexane as the eluent, to give 9.83 g of the title compound as a syrup, which solidified on being allowed to stand. The solid melted at 144°-147° C. (with decomposition and coloration at 94°-98° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646171
Source datasetuspto-grants-1997_07
ORD IDord-0499fdb7de9b421c85e4a6cf30d0c5d0
Source noteuspto-grants-1997_07