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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719997Generated: October 26, 2026

Potassium Cyanide → 4-(Pyridin-4-YL)butanenitrile

https://huagongshe.com/reaction/1719997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
Reactant4-(3-Chloropropyl)pyridineHCID 205442—
CatalystDibenzo-18-crown-6HCID 26541—
SolventAcetonitrileHCID 6342—
Product4-(Pyridin-4-YL)butanenitrileHCID 1355753184.5%

Reaction Steps

To the product of Example 21 (6.7 g, 42.9 mmol) in 300 mL of acetonitrile (CH3CN), was added potassium cyanide (KCN, 11.2 g, 171.7 mmol) and dibenzo-18-crown-6 (1.0 g, 2.8 mmol). After the reaction had been refluxed for 18 hours, it was cooled to room temperature, and stripped of all solvent under reduced pressure. The residue was partitioned between 100 mL each of water and CH2Cl2 and the aqueous phase was washed with 3×100 mL of CH2Cl2. The combined organic phase was dried (Na2SO4), filtered, and stripped of solvent to yield 6.7 g of crude product. This material was purified by HPLC on silica gel to yield 5.3 g of the title material as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05504077
Source datasetuspto-grants-1996_04
ORD IDord-34028e911a1d4e688f05758eee4b26e0
Source noteuspto-grants-1996_04