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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210089Generated: October 30, 2026

Piperidine → HCID 86749038, compound

https://huagongshe.com/reaction/2210089

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant1,3-CyclohexanedioneHCID 10434—
ReactantCinnamaldehydeHCID 637511—
SolventEthanolHCID 702—
ProductHCID 86749038HCID 86749038—

Reaction Steps

A solution of 11.2 g (0.1 mol) of 1,3-cyclohexanedione in 110 mL of ethanol was stirred at room temperature while 1 mL of piperidine was added followed by the dropwise addition of 13 mL (0.103 mol) of trans-cinnamaldehyde over a 2 min period. The resulting mixture was stirred at room temperature for 2 hr and then in an ice-bath for 1 hr. The resulting yellow slurry was filtered with suction and the solid dried under high vacuum giving 13.9 g (61.5%) of the title dione. Recrystallization of a sample of this material from ethyl acetate gave yellow solid, mp 115.5°-118° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05457124
Source datasetuspto-grants-1995_10
ORD IDord-8bbe25bb56c5402481f1f90c68e8c36f
Source noteuspto-grants-1995_10