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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 967086Generated: October 26, 2026

Sodium Hydroxide → 4-{[2-(1H-imidazo[4,5-c]quinolin-1-yl)butoxy]methyl}benzonitrile

https://huagongshe.com/reaction/967086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant4-(Bromomethyl)benzonitrileHCID 86996—
Reactant2-(1H-imidazo[4,5-c]quinolin-1-yl)-1-butanolHCID 21898023—
CatalystBenzyltrimethylammonium chlorideHCID 5963—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product4-{[2-(1H-imidazo[4,5-c]quinolin-1-yl)butoxy]methyl}benzonitrileHCID 2225451760.2%

Reaction Steps

2-(1H-imidazo[4,5-c]quinolin-1-yl)-1-butanol (3.0 g, 12.4 mmol) was added to a stirring mixture of α-bromo-p-tolunitrile (3.0 g, 15.3 mmol), sodium hydroxide (40 ml, 50%), dichloromethane (40 ml), and benzyltrimethylammonium chloride (0.02 g, 0.11 mmol). The reaction was maintained for 72 hours and then diluted with dichloromethane (100 ml) and water (100 ml). The phases were separated and the aqueous phase was extracted with additional dichloromethane (100 ml). The organic fractions were combined, washed with water, dried (MgSO4), filtered, and concentrated in vacuo. The residue was purified by flash column chromatography (silica gel, 9/1 dichloromethane/methanol, Rf 0.48) to provide 2.66 g of 4-{[2-(1H-imidazo[4,5-c]quinolin-1-yl)butoxy]methyl}benzonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06953804B2
Source datasetuspto-grants-2005_10
ORD IDord-8cf5779e5baf49d998a63e034232cb35
Source noteuspto-grants-2005_10