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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657650Generated: October 29, 2026

Piperidine → HCID 23150307, compound

https://huagongshe.com/reaction/657650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 23150319HCID 23150319—
SolventDimethylformamideHCID 6228—
ProductHCID 23150307HCID 23150307—

Reaction Steps

A suspension of potassium carbonate (369 mg) in a solution of 4-[4-(3-chloropropoxy)benzyl]cyclohexanone (250 mg) and piperidine (264 μL) in N,N-dimethylformamide (6 mL) is heated for three hours at a temperature close to 80° C., then for two days at a temperature close to 50° C. Solvent is evaporated and the residue partioned between ethyl acetate (10 mL) and water (10 mL). The organic phase is separated by decantation, washed with a saturated aqueous solution of sodium chloride, dried over magnesium sulfate, concentrated under reduced pressure and purified by column chromatography using a gradient dichloromethane/methanol/ammonia from 99/1/0.1 to 98/2/0.2 to give 270 mg of 1-{3-[4-(4-oxocyclohex-1-yl)methylphenoxy]propyl}piperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08076329B2
Source datasetuspto-grants-2011_12
ORD IDord-044688873b7f464d8e6d30ff9b356c06
Source noteuspto-grants-2011_12