HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854329Generated: October 25, 2026
Sulfoxonium, trimethyl-, iodide (1:1) → tert-Butyl 1-oxa-6-azaspiro(2.5)octane-6-carboxylate
https://huagongshe.com/reaction/854329
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfoxonium, trimethyl-, iodide (1:1) | HCID 74498 | — |
| Reactant | tert-Butyl 4-oxopiperidine-1-carboxylate | HCID 735900 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Solvent | Tetrahydrofuran dimethoxyethane | HCID 22732251 | — |
| Product | tert-Butyl 1-oxa-6-azaspiro(2.5)octane-6-carboxylate | HCID 22135564 | — |
Reaction Steps
To a solution of tert-butyl 4-oxopiperidine-1-carboxylate (0.50 g, 2.51 mmol) in THF/DME (2:1, 6 mL) at 60° C. was added trimethylsulfoxonium iodide (0.58 g, 2.63 mmol) and sodium t-butoxide (0.25 g, 2.63 mmol). The reaction mixture was stirred at 60° C. for 30 min, cooled to rt and concentrated. Water was added and the mixture was extract with EtOAc twice. The combined organics were dried over Na2SO4, filtered and concentrated. Purification on silica gel (3:1, hexanes:EtOAc) gave tert-butyl 1-oxa-6-azaspiro[2.5]octane-6-carboxylate as a clear oil that solidified upon standing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07259157B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-cae21a44277c4849a0103731f1b91da8 |
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| Source note | uspto-grants-2007_08 |
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