HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 846530Erstellt: 24. Oktober 2026
Ethyl Acetate → cis 3a,4,5,7a-tetrahydro-2(3H)-benzofuranone
https://huagongshe.com/de/reaction/846530
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | Aluminum isopropoxide | HCID 11143 | — |
| Edukt | Ethyl (2-oxo-cyclohex-3-enyl)acetate | HCID 13834278 | — |
| Edukt | Sodium 3-carboxy-2,3-dihydroxypropanoate | HCID 23690454 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | cis 3a,4,5,7a-tetrahydro-2(3H)-benzofuranone | HCID 11205783 | 86% |
Reaktionsschritte
To a solution of 13.5 g (66.0 mmoles) of aluminum isopropoxide in 100 ml of toluene was added 2.0 g (11.0 mmoles) of 6-(carbethoxymethyl)-2-cyclohexen-1-one at room temperature, and the solution was heated to 90° C. for 18 hours. The solution was cooled to room temperature, and aqueous saturated sodium hydrogen tartrate and ethyl acetate were added. The aqueous layer was extracted with ethyl acetate, and the combined ethyl acetate extracts were dried over anhydrous magnesium sulfate and evaporated under reduced pressure. The crude material was purified by Kugelrohr distillation (bp 40°-80° C./0.01 mm Hg) to yield 1.3 g (86%) of cis 3a,4,5,7a-tetrahydro-2(3H)-benzofuranone, as confirmed by NMR and IR data.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05137035 |
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| Quelldatensatz | uspto-grants-1992_08 |
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| ORD ID | ord-b2d6c0049ace41d3a351d491dc0f1323 |
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| Quellennotiz | uspto-grants-1992_08 |
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