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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1482756Erstellt: 26. Oktober 2026

Di-tert-butyl peroxide → Benzene, (cyclohexyloxy)-

https://huagongshe.com/reaction/1482756

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDi-tert-butyl peroxideHCID 8033—
EduktCyclohexaneHCID 8078—
EduktPhenyl acetateHCID 31229—
ProduktBenzene, (cyclohexyloxy)-HCID 137492—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

Into a pressure vessel phenyl acetate (126 μL, 1 mmol, 1 eq) was added and diluted with cyclohexane (1.080 mL, 10 mmol, 10 eq). To this stirring solution was added 1 mol % of a stock solution of {[Cl2NN]Cu}2(benzene) from the catalyst stock solution described in Example 4 (200 μL=0.01 mmol). After adding of tert-butyl peroxide (220 μL, 1.2 mmol), the pressure vessel was sealed and heated to 90° C. for 24 hr. The catalyst was separated by exposing the mixture to air and filtering through Celite®. After removing cyclohexane under vacuum, the residue was analyzed by 1H NMR and GC/MS to determine the yield and consumption of starting materials.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09416080B2
Quelldatensatzuspto-grants-2016_08
ORD IDord-4fcaf084be86445296ae50a01f11db1d
Quellennotizuspto-grants-2016_08