HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-Cyclopenten-1-one | HCID 13588 | — |
| Edukt | (2-Ethoxy-2-oxoethyl)dimethylsulphonium bromide | HCID 78861 | — |
| Edukt | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Edukt | Hydrochloridesodium chloride | HCID 19796930 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | ethyl (1S,5R,6S)-2-oxobicyclo[3.1.0]hexane-6-carboxylate | HCID 10725776 | 68,3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06268507B1 |
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| Quelldatensatz | uspto-grants-2001_07 |
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| ORD ID | ord-4be1601add69466a940789500845e5f8 |
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| Quellennotiz | uspto-grants-2001_07 |
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