Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1266001Generated: November 4, 2026

Hexane → Cyclopentylidenecyclopentan-2-one

https://huagongshe.com/reaction/1266001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantCyclopentanoneHCID 8452—
ReactantPotassium HydroxideHCID 14797—
SolventEthanolHCID 702—
ProductCyclopentylidenecyclopentan-2-oneHCID 6999552%

Reaction Steps

To a stirring solution of cyclopentanone (336.5 g, 4.0 moles) in absolute ethanol (500 mL) at room temperature was added KOH (5.6 g, 0.1 mole) in one portion. The reaction was stirred at room temperature for 65 hours. The reaction was determined to be completed by TLC and GC analyses. Hexane was added to the reaction mixture and the layers were separated. The organic layer was washed successively with 10% HCl (aqueous), saturated NaHCO3 (aqueous) and brine. The resulting organic layer was dried with MgSO4, filtered, and concentrated. The brown oil was distilled under vacuum to give 2-cyclopentylidenecyclopentan-1-one (155 g, 52% yield). The structural formula of 2-cyclopentylidenecyclopentan-1-one is shown in FIG. 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06548474B1
Source datasetuspto-grants-2003_04
ORD IDord-b5970edb721340e8af36571d3fcfa220
Source noteuspto-grants-2003_04