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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616218Generated: October 26, 2026

4-(9-Xanthenylidene)piperidine → 4-[4-(9-Xanthenylidene)piperidino]-2-butanone

https://huagongshe.com/reaction/616218

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(9-Xanthenylidene)piperidineHCID 15780516—
CatalystTribenzylmethyl ammonium hydroxideHCID 21829752—
SolventEthanolHCID 702—
SolventMethyl vinyl ketoneHCID 6570—
Product4-[4-(9-Xanthenylidene)piperidino]-2-butanoneHCID 20371549—

Reaction Steps

One drop of tribenzylmethyl ammonium hydroxide is added to a solution of 7 g of 4-(9-xanthenylidene)-piperidine in 70 cc of ethanol, 4.38 cc of methylvinylketone are then added dropwise, and stirring is effected at 50° for 4 hours. The reaction mixture is then concentrated by evaporation in a vacuum, the residue is dissolved in chloroform, extraction is effected with water, and after drying over magnesium sulphate, concentration is effected by evaporation. The partially crystalline residue is triturated with ether/petroleum ether 1:1 and recrystallized from ethanol. M.P. of the title compound 111°-112°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04072756
Source datasetuspto-grants-1978_02
ORD IDord-20235b3223a44cbda69c7b47faca4260
Source noteuspto-grants-1978_02