HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643536Generated: October 27, 2026
Sodium periodate → Tert-butyl 4-(3-(ethoxycarbonyl)phenyl)-2-oxopiperidine-1-carboxylate
https://huagongshe.com/reaction/643536
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium periodate | HCID 23667635 | — |
| Reactant | Tert-butyl 4-[3-(ethoxycarbonyl)phenyl]piperidine-1-carboxylate | HCID 57880576 | — |
| Catalyst | Ruthenium dioxide hydrate | HCID 16211523 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Tert-butyl 4-(3-(ethoxycarbonyl)phenyl)-2-oxopiperidine-1-carboxylate | HCID 57880492 | 29.5% |
Reaction Steps
To a stirred solution of tert-butyl 4-[3-(ethoxycarbonyl)phenyl]piperidine 1-carboxylate (48 g, 220 mmol) in chloroform (900 mL) was added ruthenium (IV) oxide hydrate (6.0 g, 45 mmol) followed by a solution of sodium periodate (150 g, 700 mmol) in water (900 m L). The resulting heterogenous reaction mixture was stirred at room temperature for 11 days before being filtered through a short column of celite. The organic layer was removed and the aqueous layer was extracted twice with DCM. The combined organic layers were washed with a 10% solution of sodium thiosulfate in water twice, and once with brine. This solution was dried over MgSO4, filtered, and concentrated under reduced pressure. The product was purified by flash chromatography (silica gel, 20% EA/hexanes) to give 22.5 g (64.8 mmol) of tert-butyl 4-[3-(ethoxycarbonyl)phenyl]-2-oxopiperidine-1-carboxylate (29%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700591B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-d8d82568766f4fe0bee0c03197bebd0d |
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| Source note | uspto-grants-2010_04 |
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