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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 133645Erstellt: 24. Oktober 2026

Hydrogen Peroxide → 1-Cyclohexyloxy-4-benzoyloxy-2,2,6,6-tetramethylpiperidine

https://huagongshe.com/de/reaction/133645

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrogen PeroxideHCID 784—
EduktAcetonitrileHCID 6342—
EduktBoric AcidHCID 7628—
Edukt1-Hydroxy-4-benzoyloxy-2,2,6,6-tetramethylpiperidineHCID 688178—
KatalysatorBoric AcidHCID 7628—
LösungsmittelWaterHCID 962—
LösungsmittelCyclohexaneHCID 8078—
Produkt1-Cyclohexyloxy-4-benzoyloxy-2,2,6,6-tetramethylpiperidineHCID 2337209868%

Reaktionsbedingungen

Temperatur52 °C

Reaktionsschritte

A solution of 0.100 g (0.360 mmol) of ferrous sulfate heptahydrate and 0.112 g (1.82 mmol) of boric acid in 4 ml of water is added to a mixture of 5.00 g (18.1 mmol) of 1-oxyl-4-benzoyloxy-2,2,6,6-tetramethylpiperidine, 27 ml of acetonitrile, and 19 ml of cyclohexane. The mixture is heated to 52° C. A solution of 4.98 g (73 mmol) of 50% aqueous hydrogen peroxide is added dropwise over 2.75 hours to the reaction mixture while the temperature is brought to and maintained at reflux (63° C.). A solution of 0.051 g of ferrous sulfate heptahydrate and 0.042 g of boric acid in 2 ml of water is added to the reaction mixture 1.25 hours after the peroxide addition is started. After the peroxide is added, the reaction mixture is heated at reflux for 30 minutes, then allowed to cool slowly. Work-up and purification according to the procedure of Example 5 afford 4.42 g (68% yield) of the title compound, a colorless syrup, GC assay 99.3%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07390904B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-3be2a870370043d3af12d94d8a753174
Quellennotizuspto-grants-2008_06