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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 133631Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/133631

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrogen PeroxideHCID 784—
EduktMethanesulfonic AcidHCID 6395—
EduktCyclohexaneHCID 8078—
Edukt1-Hydroxy-2,2,6,6-tetramethyl-4-oxopiperidineHCID 98642—
KatalysatorFerrous sulfate heptahydrateHCID 62662—
LösungsmittelMethanolHCID 887—
ProduktN-cyclohexyloxy-4-oxo-2,2,6,6-tetramethylpiperidineHCID 2201986835%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07390904B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-a53408cb0ce54faa8f117c9a7ef781f0
Quellennotizuspto-grants-2008_06