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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223933Generated: October 29, 2026

Hydrochloric Acid → 3,9-Dioxaspiro[5.5]undecan-2-one

https://huagongshe.com/reaction/2223933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHydrogen PeroxideHCID 784—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178419114HCID 178419114—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product3,9-Dioxaspiro[5.5]undecan-2-oneHCID 10487355—

Reaction Steps

To an ice-cooled solution of methyl (4-vinyltetrahydropyran-4-yl) acetate (455 mg) in tetrahydofuran (3 mL) was added 0.5M 9-borabicyclo[3.3.1]-nonane/tetrahydrofuran (10.0 mL) dropwise over 10 minutes. The reaction solution was allowed for its temperature to rise to room temperature and it was stirred for additional 17 hours. The reaction solution was again ice-cooled and ethanol (2 mL), a 6N aqueous sodium hydroxide solution (4 mL) and 30% hydrogen peroxide (4 mL) were added thereto successively. The reaction solution was then allowed for its temperature to rise to room temperature and it was stirred for additional 30 minutes. The reaction solution was again ice-cooled. After addition of conc. hydrochloric acid (2.5 mL), the reaction solution was allowed for its temperature to rise to room temperature. The solution was stirred for additional 1 hour. The reaction solution was extracted with chloroform. The organic layer was washed with saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The resulting residue was purified by chromatography [silica gel, hexane-ethyl acetate (7:3 to 6:4)] to give the title compound (271 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07375115B2
Source datasetuspto-grants-2008_05
ORD IDord-933442d242c246e08f289a4b06866db3
Source noteuspto-grants-2008_05