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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2194379Generated: November 1, 2026

Potassium Iodide → 1-(4-chlorobutyl)-4-methylpyridin-2(1H)-one

https://huagongshe.com/reaction/2194379

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Bromo-4-chlorobutaneHCID 81364—
ReactantHCID 178428601HCID 178428601—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product1-(4-chlorobutyl)-4-methylpyridin-2(1H)-oneHCID 5923464572.8%

Reaction Steps

A mixture of 2-hydroxy-4-methylpyridine (1.50 g, 13.75 mmol) and potassium carbonate (1.90 g, 13.75 mmol) in 13 ml of methanol were stirred at room temperature for 15 minutes and then 1-bromo-4-chlorobutane (3.54 g, 20.62 mmol) and a spatula tip of potassium iodide were added thereto. The reaction mixture was heated to reflux for 6 hours and then stirred at room temperature for 12 hours. Water was then added to the reaction mixture, and the aqueous mixture was extracted with dichloromethane. Drying of the organic phase and removal of the desiccant by filtration was followed by concentration of the organic phase in vacuo. Flash chromatography of resulting residue on silica gel (eluent: CH2Cl2/CH3OH: 98:2) afforded 2.0 g of 1-(4-chlorobutyl)-4-methylpyridin-2(1H)-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08334289B2
Source datasetuspto-grants-2012_12
ORD IDord-2890c12eea07458a84cc18524000dd1f
Source noteuspto-grants-2012_12