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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816964Generated: November 1, 2026

Sodium periodate → Tert-butyl 4-(3-(ethoxycarbonyl)phenyl)-2-oxopiperidine-1-carboxylate

https://huagongshe.com/reaction/1816964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium periodateHCID 23667635—
ReactantTert-butyl 4-[3-(ethoxycarbonyl)phenyl]piperidine-1-carboxylateHCID 57880576—
CatalystRuthenium dioxide hydrateHCID 16211523—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
ProductTert-butyl 4-(3-(ethoxycarbonyl)phenyl)-2-oxopiperidine-1-carboxylateHCID 5788049229.5%

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 mL). 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598243B2
Source datasetuspto-grants-2009_10
ORD IDord-a83d38ae54a840c7bccd3fddbc52d1f5
Source noteuspto-grants-2009_10