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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53023Generated: October 26, 2026

Ammonium Chloride → 2-Butyl-5-cyano-4-(1-hydroxy-1-methylethyl)-1-tritylimidazole

https://huagongshe.com/reaction/53023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Acetyl-2-butyl-5-cyano-1-tritylimidazoleHCID 19036085—
ReactantHCID 178418373HCID 178418373—
SolventTetrahydrofuranHCID 8028—
Product2-Butyl-5-cyano-4-(1-hydroxy-1-methylethyl)-1-tritylimidazoleHCID 19036221—

Reaction Conditions

Temperature40 °C

Reaction Steps

1 ml of a 2M solution of methylmagnesium iodide in tetrahydrofuran was added dropwise at room temperature, whilst stirring, to a solution of 840 mg of 4-acetyl-2-butyl-5-cyano-1-tritylimidazole [prepared as described in Preparation 5(ii)] in 15 ml of tetrahydrofuran, and the resulting mixture was stirred at 40° C. for 1 hour. The mixture was cooled, and then a saturated aqueous solution of ammonium chloride was added to it dropwise. The tetrahydrofuran layer was separated and concentrated by evaporation under reduced pressure. The concentrate was purified by column chromatography through silica gel, using a 2:1 by volume mixture of hexane and ethyl acetate as the eluent, to give 539 mg of the title compound as a colorless solid, melting at 151°-152° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616599
Source datasetuspto-grants-1997_04
ORD IDord-56c2775e83704fca903ab9751772b843
Source noteuspto-grants-1997_04