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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1266002Generated: November 1, 2026

Water → HCID 15304482, compound

https://huagongshe.com/reaction/1266002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAllyl chlorideHCID 7850—
ReactantSodium hydrideHCID 24758—
ReactantCyclopentylidenecyclopentan-2-oneHCID 69995—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15304482HCID 1530448269%

Reaction Steps

To a stirring solution of 2-cyclopentylidenecyclopentan-1-one (62.5 g, 0.417 moles) in dry THF (450 mL) at room temperature under nitrogen, was added NaH (60% oil dispersion, 20.0 g, 0.5 moles) in one portion. The mixture was stirred at room temperature for 30 min and then a solution of allyl chloride (38.3 g, 0.5 moles) in THF (100 mL) was added dropwise over 30 min. When the addition was complete, the reaction was warmed gently to approximately 40° C. It was determined by TLC and GC that the reaction was complete after 18 hours. Water was added to the reaction mixture and the layers were separated, with the organic layer being 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-cyclopent-1-enyl-2-prop-2-enylcyclopentan-1-one (54.5 g, 69.0% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06548474B1
Source datasetuspto-grants-2003_04
ORD IDord-62dac055f7f047679bc8ad1d6c93b823
Source noteuspto-grants-2003_04