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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1765Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/1765

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Cyclopenten-1-oneHCID 13588—
Edukt(2-Ethoxy-2-oxoethyl)dimethylsulphonium bromideHCID 78861—
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
EduktHydrochloridesodium chlorideHCID 19796930—
LösungsmittelTolueneHCID 1140—
ProduktEthyl 2-oxobicyclo[3.1.0]hexane-6-carboxylateHCID 56535768,3%

Reaktionsschritte

A suspension of carboethoxymethyl dimethylsulfonium 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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05726320
Quelldatensatzuspto-grants-1998_03
ORD IDord-8fef71afc98949c49bc84e25d6876698
Quellennotizuspto-grants-1998_03