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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586962Generated: November 1, 2026

Acetone → 1-Methyl-1-azaspiro[4.5]decane-2,8-dione

https://huagongshe.com/reaction/1586962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantHydrochloric AcidHCID 313—
ReactantSodium IodideHCID 5238—
ReactantHCID 54503705HCID 54503705—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product1-Methyl-1-azaspiro[4.5]decane-2,8-dioneHCID 15229685—

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 3-Mesyloxy-1-methyl-1-azaspiro[4.5]decane-2,8-dione ethylene ketal (1.28 g), sodium iodide (1.8 g) and acetone (20 mL) was refluxed with stirring for 90 min. The solvent was removed in vacuo and the residue was dissolved in methylene chloride and washed with water. After drying over magnesium sulfate the solvent was removed in vacuo. The residue was dissolved in toluene (20 mL) and treated with tri-n-butyltin hydride (1.75 g) and AIBN (20 mg) and the resulting mixture was heated at 110° C. for 1 h. After removal of the solvent the residue was chromatographed on silica gel with ethyl acetate as the eluent. The resulting produce was stirred with a mixture of water (5 mL), 3N HCl (1.5 mL) and acetic acid (2 mL) for 16 h. The resulting product was extracted 3 times with methylene chloride, washed with sodium bicarbonate solution, dried over magnesium sulfate and the solvent was removed in vacuo to afford 1 -Methyl-1-azaspiro[4.5]decane-2,8-dione as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05216159
Source datasetuspto-grants-1993_06
ORD IDord-b25ff6e0981b44ed9abd4910294d3460
Source noteuspto-grants-1993_06