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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434005Generated: October 26, 2026

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

https://huagongshe.com/reaction/434005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant3-Bromo-4-methylbenzonitrileHCID 14004840—
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 cc-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, Rf0.48) 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 numberUS06670372B2
Source datasetuspto-grants-2003_12
ORD IDord-e012e80795af4fd1b38d7c43054bad18
Source noteuspto-grants-2003_12