Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846530Generated: October 25, 2026

Ethyl Acetate → cis 3a,4,5,7a-tetrahydro-2(3H)-benzofuranone

https://huagongshe.com/reaction/846530

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantAluminum isopropoxideHCID 11143—
ReactantEthyl (2-oxo-cyclohex-3-enyl)acetateHCID 13834278—
ReactantSodium 3-carboxy-2,3-dihydroxypropanoateHCID 23690454—
SolventTolueneHCID 1140—
Productcis 3a,4,5,7a-tetrahydro-2(3H)-benzofuranoneHCID 1120578386%

Reaction Conditions

Temperature90 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05137035
Source datasetuspto-grants-1992_08
ORD IDord-b2d6c0049ace41d3a351d491dc0f1323
Source noteuspto-grants-1992_08