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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 744073Generated: October 30, 2026

3-Cyanophenol → HCID 178509864, compound

https://huagongshe.com/reaction/744073

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-CyanophenolHCID 13394—
ReactantSodium hydrideHCID 24758—
Reactant4-(2-chloroethyl)-1H-imidazole hydrochlorideHCID 178478570—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDimethylformamideHCID 6228—
ProductHCID 178509864HCID 178509864—

Reaction Steps

240 mg (60% in oil; 6 mmol) of sodium hydride are added to a solution of 1.43 g (12 mmol) of 3-hydroxybenzonitrile in 10 ml of dimethylformamide and the mixture is stirred at room temperature for 1 hour under nitrogen. 200 mg (1.2 mmol) of 4-(2-chloroethyl)-1H-imidazole hydrochloride and tetrabutylammonium iodide (catalytic amount) are added and the mixture is heated for 3 hours at 80° C. The solvent is evaporated under reduced pressure and the oily residue is stirred in ethanol and filtered. The filtrate is evaporated and the residue is purified by chromatography on a column of silica gel (first eluent chloroform, second eluent 95/5 chloroform/methanol). The title compound is converted to the oxalate and crystallized from a 2/1 ethanol/diethyl ether mixture, M.p.: 189°-190° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05559113
Source datasetuspto-grants-1996_09
ORD IDord-8f1e5384efcc4165aa0e1057039a3859
Source noteuspto-grants-1996_09