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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 265167Generated: October 29, 2026

Ethyl Acetate → 2-Butyl-5-cyano-4-(1-hydroxy-1-methylpropyl)-1-tritylimidazole

https://huagongshe.com/reaction/265167

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Butyl-5-cyano-4-propionyl-1-tritylimidazoleHCID 19036190—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
Product2-Butyl-5-cyano-4-(1-hydroxy-1-methylpropyl)-1-tritylimidazoleHCID 19036197—

Reaction Conditions

Temperature30 °C

Reaction Steps

5 ml of a 1M solution of methylmagnesium bromide in tetrahydrofuran were added dropwise at 10° C. under an atmosphere of nitrogen to a solution of 2 g of 2-butyl-5-cyano-4-propionyl-1-tritylimidazole (prepared as described in Preparation 15) in 36 ml of tetrahydrofuran, and the resulting mixture was stirred at 20° C. for 1 hour and subsequently at 30° C. for a further 1 hour. At the end of this time, a mixture of a saturated aqueous solution of ammonium chloride and ethyl acetate was added to the reaction mixture, which was then well shaken. The ethyl acetate layer was separated and dried over anhydrous magnesium sulfate. After the drying agent had been removed by filtration, the solvent was distilled off under reduced pressure. The residue was purified by column chromatography through silica gel, using a 1:2 by volume mixture of ethyl acetate and hexane as the eluent, to give 1.29 g of the title compound as crystals, melting at 90°-93° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646171
Source datasetuspto-grants-1997_07
ORD IDord-2526db14dae144608a136b13e7fabc4d
Source noteuspto-grants-1997_07