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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 744072Generated: October 27, 2026

Sodium hydride → HCID 178436664, compound

https://huagongshe.com/reaction/744072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-EthylphenolHCID 31242—
Reactant4-(2-chloroethyl)-1H-imidazole hydrochlorideHCID 178478570—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDimethylformamideHCID 6228—
ProductHCID 178436664HCID 178436664—

Reaction Steps

180 mg (60% in oil; 4.5 mmol) of sodium hydride are slowly added to a solution of 1.1 g (9 mmol) of 4-ethylphenol in 7 ml of dimethylformamide and the mixture is stirred at room temperature for 2 hours. 150 mg (0.9 mmol) of 4-(2-chloroethyl)-1H-imidazole hydrochloride and tetrabutylammonium iodide (catalyst) are added and the mixture is stirred at 80° C. for 3 days. The solvent is concentrated and 50 ml of diethyl ether are added. The precipitate is separated by filtration and the filtrate is evaporated under reduced pressure to give a residue which is subjected to column chromatography through silica gel (first eluent ethyl acetate, second eluent 95/5 ethyl acetate/methanol). The title compound is then purified by preparative chromatography and then converted to the oxalate which, after crystallization from an ethanol/diethyl ether mixture, melts at 178° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05559113
Source datasetuspto-grants-1996_09
ORD IDord-126a99dfe99c411d8c24ffd650bddae5
Source noteuspto-grants-1996_09