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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249662Generated: October 30, 2026

Ethyl Acetate → 8-(3-Methylbutylidene)-1,4-dioxaspiro[4.5]decane

https://huagongshe.com/reaction/2249662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant1,4-Dioxaspiro[4.5]decan-8-oneHCID 567415—
Reactant(3-Methylbutyl)(triphenyl)phosphanium iodideHCID 22245250—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product8-(3-Methylbutylidene)-1,4-dioxaspiro[4.5]decaneHCID 6898719078%

Reaction Steps

In 100 ml of tetrahydrofuran is suspended 39.8 g of isopentyltriphenylphosphonium iodide. At −25° C. to −20° C., 52 ml of a 1.6 mol/L solution of n-butyllithium in n-hexane is dropwise added to the suspension. After stirring the mixture thus obtained at −25° C. to −15° C. for one hour, the temperature is elevated to ambient temperature over a period of one hour. A solution of 10.0 g of 1,4-dioxaspiro[4.5]-decan-8-one in 50 ml of tetrahydrofuran is added to the reaction mixture and stirred at ambient temperature for one hour. The reaction mixture is added to a mixture of ethyl acetate and water, and the organic layer is separated. The organic layer thus obtained is washed with water and saturated aqueous solution of sodium chloride successively and dried over anhydrous magnesium sulfate, and then the solvent is distilled off under reduced pressure. The residue thus obtained is purified by silica gel column chromatography (eluent; n-hexane:ethyl acetate=95:5) to obtain 10.5 g of 8-(3-methylbutylidene)-1,4-dioxaspiro[4.5]decane as a colorless oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07314888B1
Source datasetuspto-grants-2008_01
ORD IDord-1c69f187b66b4b009de285e49dcb8351
Source noteuspto-grants-2008_01