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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416328Generated: October 26, 2026

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

https://huagongshe.com/reaction/1416328

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Cyclopenten-1-oneHCID 13588—
Reactant(2-Ethoxy-2-oxoethyl)dimethylsulphonium bromideHCID 78861—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHydrochloridesodium chlorideHCID 19796930—
SolventTolueneHCID 1140—
ProductEthyl 2-oxobicyclo[3.1.0]hexane-6-carboxylateHCID 56535768.3%

Reaction Steps

A suspension of carboethoxymethyl dimethylsulfonium bromide (45.5 g, 198.6 mmol) in toluene (350 mL) was treated with 1,8-diazabicyclo[5.4.0]undec-7-ene (30.2 g, 198.4 mmol). The resulting mixture was stirred at room temperature. After one hour, the reaction mixture was treated with 2-cyclopenten-1-one (19.57 g, 238.4 mmol). After an additional 18 hours, the reaction mixture was added to a 1 N 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 (68%) of the title compound. Melting point: 36-38° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05912248
Source datasetuspto-grants-1999_06
ORD IDord-6c3bafc0564c460c9b8ed3202162e292
Source noteuspto-grants-1999_06