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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177902Generated: October 29, 2026

Benzyl Alcohol → 6-(Benzyloxy)pyridine-3-carbonitrile

https://huagongshe.com/reaction/1177902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantPotassium HydroxideHCID 14797—
Reactant6-Chloro-3-pyridinecarbonitrileHCID 5152094—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product6-(Benzyloxy)pyridine-3-carbonitrileHCID 2470010640.3%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a stirred solution of 6-chloronicotinonitrile (1 g, 7.2 mmol) and benzyl alcohol (780 mg, 7.2 mmol) in toluene (15 mL) was added KOH (729 mg, 12.99 mmol) and 18 crown ether (2.86 g, 10.8 mmol). The resulting mixture was stirred at 70° C. for 7 hrs. The mixture was diluted with cold water and the product was extracted with EtOAc. The organic layer was washed with saturated brine solution and dried over Na2SO4. The organic layer was then concentrated under reduced pressure. The obtained residue was purified by column chromatography (using neutral alumina and 5% MeOH: CHCl3 as eluent) to afford 610 mg (40.1% yield) of 6-benzyloxy-nicotinonitrile. LCMS Purity: 77.69%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842696B2
Source datasetuspto-grants-2010_11
ORD IDord-19efeb69868d4291a959ed5671a38cef
Source noteuspto-grants-2010_11