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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413917Generated: October 26, 2026

Acetic Acid → 2-(2-Piperidinylidene)-acetophenone

https://huagongshe.com/reaction/1413917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodiumHCID 5360545—
Reactant1-phenyl-2-piperidin-2-ylidenebutane-1,3-dioneHCID 178467972—
SolventEthanolHCID 702—
Product2-(2-Piperidinylidene)-acetophenoneHCID 70574154—

Reaction Steps

12.15 g (0.05 mole) of 1-phenyl-2-(2-piperidinylidene)-1,3-butanedione are introduced into a prepared solution of 3.5 g of sodium in 120 ml of ethanol. The reaction mixture is then refluxed for 40 minutes. After cooling, it is neutralised with glacial acetic acid, and filtered off from the sodium acetate. The filtrate is concentrated in the rotary evaporator, and the residue is dissolved in methylene chloride. The solution is repeatedly extracted with water; the organic phase is dried over sodium sulphate, and the solvent is evaporated off in the rotary evaporator. The oily residue is crystallised from ether/hexane to yield 2-(2-piperidinylidene)-acetophenone, m.p. 59°-60°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04251542
Source datasetuspto-grants-1981_02
ORD IDord-281070d595ce4ba99d082497ab901105
Source noteuspto-grants-1981_02