Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2386943Generated: November 1, 2026

Cyclopentanone → HCID 23151368, compound

https://huagongshe.com/reaction/2386943

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentanoneHCID 8452—
Reactant4-(4-Nitrophenoxy)piperidineHCID 21918653—
SolventMethanolHCID 887—
SolventZincchlorideHCID 3007855—
SolventSodium cyanoborohydrideHCID 5003444—
ProductHCID 23151368HCID 2315136897%

Reaction Steps

4-(4-nitrophenoxy)piperidine (1.03 g, 4.65 mmol) and cyclopentanone (783 mg, 9.31 mmol) were dissolved in a 0.5M methanol solution (20 mL) of zinc(II) chloride and sodium cyanoborohydride, and stirred at room temperature for 10 hours. The solvent was distilled off under reduced pressure, ethyl acetate and 1N sodium hydroxide aqueous solution were added, the mixture was extracted with ethyl acetate, and the organic phase washed with distilled water. After drying with anhydrous sodium sulfate, the product was concentrated, and the target compound (1.31 g, 96%) was thereby obtained as a light brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268842B2
Source datasetuspto-grants-2012_09
ORD IDord-5bab6e5080054a1bbc0c1a3a118f785a
Source noteuspto-grants-2012_09