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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133631Generated: October 26, 2026

Hydrogen Peroxide → N-cyclohexyloxy-4-oxo-2,2,6,6-tetramethylpiperidine

https://huagongshe.com/reaction/133631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantMethanesulfonic AcidHCID 6395—
ReactantCyclohexaneHCID 8078—
Reactant1-Hydroxy-2,2,6,6-tetramethyl-4-oxopiperidineHCID 98642—
CatalystFerrous sulfate heptahydrateHCID 62662—
SolventMethanolHCID 887—
ProductN-cyclohexyloxy-4-oxo-2,2,6,6-tetramethylpiperidineHCID 2201986835%

Reaction Steps

A solution of 20.1 g (0.295 mol) of 50% aqueous hydrogen peroxide is added over 6 hours at 60° C. to a mixture of 8.51 g (50.0 mmol) of 1-oxyl-2,2,6,6-tetramethylpiperid-4-one, 0.70 g (2.5 mmol) of iron(II) sulfate heptahydrate, 0.3 ml (5 mmol) of methanesulfonic acid, 11 ml of cyclohexane, and 90 ml of methanol. Shortly after the addition is completed, the reaction mixture tests negative for hydrogen peroxide. The reaction mixture is concentrated to afford 4.4 g (35% yield) of the title compound, isolated as a yellow oil. Structure is confirmed by mass spectrometry and NMR analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07390904B2
Source datasetuspto-grants-2008_06
ORD IDord-a53408cb0ce54faa8f117c9a7ef781f0
Source noteuspto-grants-2008_06