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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2258553Generated: October 30, 2026

2-Cyclopenten-1-one → Ethyl 2-oxobicyclo[3.1.0]hexane-6-carboxylate

https://huagongshe.com/reaction/2258553

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Cyclopenten-1-oneHCID 13588—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHydrochloridesodium chlorideHCID 19796930—
ReactantHCID 86751185HCID 86751185—
SolventTolueneHCID 1140—
ProductEthyl 2-oxobicyclo[3.1.0]hexane-6-carboxylateHCID 56535776.7%

Reaction Steps

A suspension of carbethoxymethyl diethylsulfonium bromide (45.5 g) in toluene (350 mL) was treated with 1,8-diazabicyclo[5.4.0]undec-7-ene (30.2 g). The resulting mixture was stirred at room temperature. After one hour, the reaction mixture was treated with 2-cyclopenten-1-one (19.57 g). After an additional 18 hours, the reaction mixture was added to a 1N hydrochloric acid/sodium chloride solution. The resulting mixture was extracted with diethyl ether. The combined ether extracts were dried over magnesium sulfate, filtered, and concentrated in vacuo. The residue was purified using silica-gel chromatography, eluting with a linear gradient of 10% ethyl acetate/hexanes to 50% ethyl acetate/hexanes, to give 22.81 g of the title compound. Melting point: 36°-38° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05661184
Source datasetuspto-grants-1997_08
ORD IDord-83eb286c76ba4f76a67c26a3eae7c8a0
Source noteuspto-grants-1997_08