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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2083188Generated: October 26, 2026

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

https://huagongshe.com/reaction/2083188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantHydrochloric AcidHCID 313—
Reactant1-Methyl-4-piperidoneHCID 74049—
SolventEthanolHCID 702—
Product4-Piperidinone, 1-methyl-3,5-bis(phenylmethylene)-, hydrochlorideHCID 358708—

Reaction Steps

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.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04085102
Source datasetuspto-grants-1978_04
ORD IDord-f4b108035e4041fe9bea41b7f669e775
Source noteuspto-grants-1978_04