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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1810776Generated: November 1, 2026

2-Piperidone → 1-(4-Methoxybenzyl)piperidin-2-one

https://huagongshe.com/reaction/1810776

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PiperidoneHCID 12665—
ReactantPotassium HydroxideHCID 14797—
Reactant4-Methyloxybenzyl chlorideHCID 69993—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTolueneHCID 1140—
Product1-(4-Methoxybenzyl)piperidin-2-oneHCID 1150680152.1%

Reaction Steps

A suspension of potassium hydroxide (85%, 18.6 g) and tetrabutylammonium bromide (4.88 g) in toluene (250 ml) was refluxed overnight under nitrogen atmosphere using Deenschtark device. The mixture was cooled to 80° C., to which a solution of 2-piperidone (25.0 g) and 4-methoxybenzylchloride (51.3 g) in toluene (50 ml) were added dropwise. After refluxing for 8 hours, the reaction mixture was returned to room temperature and washed with water and saturated brine. The resultant was dried with magnesium sulfate, after which the solvent was distilled off under reduced pressure, and the resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1) to give 1-(4-methoxybenzyl)piperidin-2-one (28.8 g) as a colorless oily material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362058B2
Source datasetuspto-grants-2013_01
ORD IDord-79bcaf0de24f418abf078a5825988026
Source noteuspto-grants-2013_01