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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172194Generated: October 31, 2026

1,4-Cyclohexanedione → HCID 70873346, compound

https://huagongshe.com/reaction/2172194

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-CyclohexanedioneHCID 12511—
Reactant4-(3,4-Dichlorophenoxy)piperidineHCID 3732042—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 70873346HCID 7087334653.3%

Reaction Conditions

Temperature55 °C

Reaction Steps

10% palladium on carbon (350 mg) was added to an ethanol solution (50 ml) of 4-(3,4-dichlorophenoxy)piperidine (7.1 g) and 1,4-cyclohexanedione (6.47 g), and the mixture was stirred at 50 to 60° C. for 5 hours. After being cooled to room temperature, the catalyst was removed by filtration, and the filtrate was concentrated under reduced pressure. The residue was dissolved in ethyl acetate, washed with a saturated sodium chloride aqueous solution, and dried over magnesium sulfate. After being concentrated under reduced pressure, the residue was purified by silica gel column chromatography (hexane:ethyl acetate=9:1→3:1) to afford the title compound as a pale brown powder (5.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051333B2
Source datasetuspto-grants-2015_06
ORD IDord-822f3477d8f94f88800a621ba63096a9
Source noteuspto-grants-2015_06