Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172186Generated: October 31, 2026

1,4-Cyclohexanedione → HCID 67275119, compound

https://huagongshe.com/reaction/2172186

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-CyclohexanedioneHCID 12511—
ReactantHCID 23081575HCID 23081575—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 67275119HCID 6727511917.6%

Reaction Conditions

Temperature75 °C

Reaction Steps

10% palladium on carbon (64 mg) was added to an ethanol solution (13 ml) of 4-(4-trifluoromethoxybenzyl)piperidine (1.28 g) and 1,4-cyclohexanedione (1.19 g), and the mixture was stirred at 70 to 80° C. for 8.5 hours. After being cooled to room temperature, the catalyst was removed by filtration, and the filtrate was concentrated under reduced pressure. After being dissolved in ethyl acetate, the residue was 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=10:0→6:4) to afford the title compound as a black oil (305 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051333B2
Source datasetuspto-grants-2015_06
ORD IDord-cf96a904f7bc4cee9e8328e307e9cf53
Source noteuspto-grants-2015_06