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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktAluminum isopropoxideHCID 11143—
EduktEthyl (2-oxo-cyclohex-3-enyl)acetateHCID 13834278—
EduktSodium 3-carboxy-2,3-dihydroxypropanoateHCID 23690454—
LösungsmittelTolueneHCID 1140—
Produktcis 3a,4,5,7a-tetrahydro-2(3H)-benzofuranoneHCID 1120578386%

Reaktionsbedingungen

Temperatur90 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05137035
Quelldatensatzuspto-grants-1992_08
ORD IDord-b2d6c0049ace41d3a351d491dc0f1323
Quellennotizuspto-grants-1992_08