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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 331226Generated: October 25, 2026

Ethanol → 1-(1,2,2a,3,4,5-Hexahydroacenaphthylen-1-yl)piperidin-4-one

https://huagongshe.com/reaction/331226

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Ethyl-1-methyl-4-oxopiperidin-1-ium iodideHCID 11097568—
Reactant1,2,2a,3,4,5-Hexahydroacenaphthylen-1-amineHCID 63821374—
SolventWaterHCID 962—
Product1-(1,2,2a,3,4,5-Hexahydroacenaphthylen-1-yl)piperidin-4-oneHCID 6870667114%

Reaction Steps

To a mixture of 1,2,2a,3,4,5-hexahydroacenaphthylen-1-ylamine, potassium carbonate (3.89 g) and ethanol (60 ml) was added 1-ethyl-1-methyl-4-oxopiperidinium iodide (8.36 g) dissolved in water (15 ml), and the mixture was heated under reflux for 2 hr. The reaction mixture was poured into water, and the mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine, dried over magnesium sulfate, and concentrated. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give 1-(1,2,2a,3,4,5-hexahydroacenaphthylen-1-yl)piperidin-4-one (1.01 g, 14%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877779B2
Source datasetuspto-grants-2014_11
ORD IDord-27bbfc698e0847b9a4e7cddf3b391f15
Source noteuspto-grants-2014_11