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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Cyclopenten-1-one | HCID 13588 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | Hydrochloridesodium chloride | HCID 19796930 | — |
| Reactant | HCID 86751185 | HCID 86751185 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethyl 2-oxobicyclo[3.1.0]hexane-6-carboxylate | HCID 565357 | 76.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05661184 |
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| Source dataset | uspto-grants-1997_08 |
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| ORD ID | ord-83eb286c76ba4f76a67c26a3eae7c8a0 |
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| Source note | uspto-grants-1997_08 |
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