Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 263338Generated: October 31, 2026

Sodium Hydroxide → 1-[(4-Methoxyphenyl)methyl]-3-methylidenepiperidin-2-one

https://huagongshe.com/reaction/263338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactantmethyl N-(p-methoxybenzyl)nipecotate hydrochlorideHCID 14181476—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product1-[(4-Methoxyphenyl)methyl]-3-methylidenepiperidin-2-oneHCID 1277442371.4%

Reaction Steps

A solution of methyl N-(p-methoxybenzyl)nipecotate hydrochloride (30.7 g) and 8.4 g of sodium hydroxide in 900 ml of methanol and 45 ml of water is stirred at room temperature for seventeen hours. The solution is evaporated to dryness in vacuo, the residue diluted with toluene, and this again evaporated to dryness in vacuo. To the residue is added 1 liter of acetic anhydride and 140 ml of triethylamine, and the resulting mixture is heated under reflux for four hours. The reaction mixture is evaporated to dryness in vacuo, the residue taken up in chloroform, washed with water, dried, and concentrated in vacuo. The residual oil is chromatographed on silica gel using 1:1 hexane-ethyl acetate as the eluant, and yields 16.9 g of 1-(p-methoxybenzyl)-3-methylene-2-piperidone as a chromatographically pure yellow oil. Alternatively, the oil can be distilled to give analytically pure 1-(p-methoxybenzyl)-3-methylene-2-piperidone, b.p. 145°-155°/0.05 mm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04156786
Source datasetuspto-grants-1979_05
ORD IDord-60cf461aa0f444618b924b4072b46375
Source noteuspto-grants-1979_05