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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1413916Erstellt: 26. Oktober 2026

Benzoylacetone → 1-phenyl-2-piperidin-2-ylidenebutane-1,3-dione

https://huagongshe.com/reaction/1413916

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoylacetoneHCID 7166—
Edukt2-Ethoxy-3,4,5,6-tetrahydropyridineHCID 12210255—
Produkt1-phenyl-2-piperidin-2-ylidenebutane-1,3-dioneHCID 178467972—

Reaktionsschritte

12.7 g (0.1 mole) of 2-ethoxy-3,4,5,6-tetrahydropyridine and 24.4 g (0.15 mole) of 1-phenyl-1,3-butanedione are mixed and heated together in a nitrogen atmosphere, with stirring, for 32 hours in an oil bath at 100°. The reaction mixture is cooled, and subsequently chromatographed on silica gel with an ethyl acetate/hexane mixture as the eluant. The main fractions are combined and crystallised from ether to obtain 1-phenyl-2-(2-piperidinylidene)-1,3-butanedione in the form of yellow crystals, m.p. 80-81°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04251542
Quelldatensatzuspto-grants-1981_02
ORD IDord-831bd4b15cb74da599c7b154e7f5c9a3
Quellennotizuspto-grants-1981_02