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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732245Generated: October 30, 2026

Acetonitrile → 4-((5-Chloropentyl)oxy)benzonitrile

https://huagongshe.com/reaction/732245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPotassium CarbonateHCID 11430—
Reactant4-CyanophenolHCID 13019—
Reactant1-Bromo-5-chloropentaneHCID 96070—
SolventEthyl AcetateHCID 8857—
Product4-((5-Chloropentyl)oxy)benzonitrileHCID 1938151090%

Reaction Steps

While 70 g of 4-hydroxybenzonitrile (7) were added to 500 ml of acetonitrile and stirred, 85.3 g of potassium carbonate and 77.4 ml of 1-bromo-5-chloropentane were added. Subsequently, the temperature was gradually increased and stirring under reflux was continued for 8 hr, and then stirring was further continued at room temperature for 18 hr. After the reaction was completed, the resultant reaction mixture was added with 500 ml of ethylacetate and then washed with water. Thereafter, the ethylacetate layer was dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The concentrated compound was dissolved in 280 ml of methanol, stirred at 0° C. for 2 hr, and then filtered, thus obtaining 118 g (yield: 90%) of a title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585979B2
Source datasetuspto-grants-2009_09
ORD IDord-225054464824456abd76b61186e45866
Source noteuspto-grants-2009_09