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HRID 2083188Erstellt: 26. Oktober 2026

Benzaldehyde → 4-Piperidinone, 1-methyl-3,5-bis(phenylmethylene)-, hydrochloride

https://huagongshe.com/reaction/2083188

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzaldehydeHCID 240—
EduktHydrochloric AcidHCID 313—
Edukt1-Methyl-4-piperidoneHCID 74049—
LösungsmittelEthanolHCID 702—
Produkt4-Piperidinone, 1-methyl-3,5-bis(phenylmethylene)-, hydrochlorideHCID 358708—

Reaktionsschritte

A solution of 57.0 g. (0.5 mole) of 1-methyl-4-piperidinone and 106.0 g. (1.0 mole) of benzaldehyde in 400 ml. of ethanol is cooled in an ice bath and treated with HCl gas until 250 g. is absorbed. The red-colored solution is allowed to stand at room temperature overnight. The resulting deep red-brown solution is seeded, allowed to stand overnight at room temperature, and the crystalline solid is filtered on a sintered-glass funnel and washed with cold ethanol, followed by ether. After drying in a desiccator, the solid (146 g.) is digested in 400 ml. of hot ethanol (75°), cooled and filtered to give 120 g. of pale yellow product, m.p. 242-244° (dec.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04085102
Quelldatensatzuspto-grants-1978_04
ORD IDord-f4b108035e4041fe9bea41b7f669e775
Quellennotizuspto-grants-1978_04