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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374361Generated: October 26, 2026

Water → Ethyl 8-oxo-1,4-dioxaspiro[4.5]decane-7-carboxylate

https://huagongshe.com/reaction/1374361

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiethyl CarbonateHCID 7766—
ReactantSodium hydrideHCID 24758—
Reactant1,4-Dioxaspiro[4.5]decan-8-oneHCID 567415—
SolventAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductEthyl 8-oxo-1,4-dioxaspiro[4.5]decane-7-carboxylateHCID 559688—

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium hydride (60% dispersion; 45 g, 1.17 mol) was washed with 500 ml of hexane (2×), suspended in 750 mL of THF and treated with diethylcarbonate (112.5 g, 0.94 mol). The suspension was heated to reflux and treated drop-wise with a solution of 1,4-cyclohexanedione mono-ethylene ketal (60.0 g , 0.384 mol) in THF (250 mL). After the addition was complete the suspension was heated to reflux for an additional 4 hours. The mixture was cooled in an ice bath to 0° C. and then poured, while vigorously stirring, into a mixture of ice (1 L), water (100 mL) and acetic acid (100 mL). The resulting mixture was extracted with hexane (2 L total) and the extracts washed with water and brine. The hexane extract was dried over Na2SO4, filtered and concentrated to give 8-Oxo-1,4-dioxa-spiro[4.5]decane-7-carboxylic acid ethyl ester as a pale yellow oil. This was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07163937B2
Source datasetuspto-grants-2007_01
ORD IDord-dc5d2cf0cb75406e84b9a287901ddb07
Source noteuspto-grants-2007_01