HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452022Generated: October 30, 2026
Sodium Iodide → 1-Methyl-1-azaspiro[4.5]decane-2,8-dione
https://huagongshe.com/reaction/1452022
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | HCID 54503705 | HCID 54503705 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-Methyl-1-azaspiro[4.5]decane-2,8-dione | HCID 15229685 | — |
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 product 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05606059 |
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| Source dataset | uspto-grants-1997_02 |
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| ORD ID | ord-1c6279ec3cff4adca3ccc6872fb1bd6c |
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| Source note | uspto-grants-1997_02 |
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