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HRID 1387699Erstellt: 23. Oktober 2026

2-Cyclopenten-1-one → ethyl (1S,5R,6S)-2-oxobicyclo[3.1.0]hexane-6-carboxylate

https://huagongshe.com/de/reaction/1387699

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 (1S,5R,6S)-2-oxobicyclo[3.1.0]hexane-6-carboxylateHCID 1072577668,3%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06268507B1
Quelldatensatzuspto-grants-2001_07
ORD IDord-4be1601add69466a940789500845e5f8
Quellennotizuspto-grants-2001_07