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HRID 1729112Erstellt: 25. Oktober 2026

tert-Butyl hydroperoxide → 2,3-Epoxy-5-(perfluorooctyl)bicyclo[2.2.1]heptane

https://huagongshe.com/reaction/1729112

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-Butyl hydroperoxideHCID 6410—
EduktCyclopentadieneHCID 7612—
Edukt1H,1H,2H-Perfluoro-1-deceneHCID 88990—
LösungsmittelTolueneHCID 1140—
LösungsmittelHexaneHCID 8058—
Produkt2,3-Epoxy-5-(perfluorooctyl)bicyclo[2.2.1]heptaneHCID 19013695—

Reaktionsschritte

128 g (250 mmol) of the Diels-Alder reaction product of 3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluoro-1-decene (perfluorooctylethene) and cyclopentadiene are mixed in 10 ml of dry toluene with 815 mg (2.5 mmol) of molybdenum acetylacetonate, and 104 ml of a 3.6 molar solution of t-butyl hydroperoxide in toluene (375 mmol) is added dropwise at 28° C. within 2 hours. During this period, the temperature rises to 40° C. The solution is then held at 65°C. for 14 hours, and subsequently at 80° C. for another 2 hours. Thereaction mixture is filtered over magnesium silicate, followed by washing with two 20 ml portions of toluene. The low-boiling components are stripped off on a rotary evaporator. The residue obtained is taken up in 50 ml of hexane and left to crystallize for 12 hours at -28° C. Theresulting slurry of solids is filtered off with suction and dried at room temperature in an oil pump vacuum.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05331084
Quelldatensatzuspto-grants-1994_07
ORD IDord-2610e4cffb77408288eba02348538843
Quellennotizuspto-grants-1994_07