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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387181Generated: November 1, 2026

2-Naphthol → HCID 178419960, compound

https://huagongshe.com/reaction/1387181

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NaphtholHCID 8663—
ReactantSodium hydrideHCID 24758—
Reactant4-(2-chloroethyl)-1H-imidazole hydrochlorideHCID 178478570—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDimethylformamideHCID 6228—
ProductHCID 178419960HCID 178419960—

Reaction Steps

240 mg (60% in oil, 6 mmol) of sodium hydride are added to a solution of 1.73 g (12 mmol) of 2-naphthol in 10 ml of dimethylformamide. The mixture is stirred at room temperature for 3 hours 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 at 100° C. for 3 days and then the solvent is evaporated under reduced pressure. The excess 2-naphthol is extracted with diethyl ether under acidic conditions (dilute hydrochloric acid). The aqueous solution is basified with potassium carbonate and the product is extracted with diethyl ether. The ethereal extracts are concentrated and the residue obtained is crystallized from a methanol/water (½) mixture, M.p.: 157°-158° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE037303E1
Source datasetuspto-grants-2001_07
ORD IDord-0594d29243eb4e2ab00482ebc3762665
Source noteuspto-grants-2001_07