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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 992167Erstellt: 26. Oktober 2026

Toluene → 13,13,13,12,12,11,11,10,10,9,9,8,8,7,7,6,6-Heptadecafluoro-3-oxatridecanoic acid-t-butyl ester

https://huagongshe.com/reaction/992167

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
Edukt1,1,2,2-Tetrahydroperfluoro-1-decanolHCID 69619—
Edukttert-Butyl bromoacetateHCID 79177—
KatalysatorTetrabutylammonium hydrogen sulfateHCID 94433—
LösungsmittelPotassium HydroxideHCID 14797—
Produkt13,13,13,12,12,11,11,10,10,9,9,8,8,7,7,6,6-Heptadecafluoro-3-oxatridecanoic acid-t-butyl esterHCID 22352715—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

10.51 g (53.9 mmol) of bromoacetic acid-tert-butyl ester is added in drops to a mixture of 10 g (21.55 mmol) of 1H,1H,2H,2H-perfluorodecan-1-ol and 0.73 g (2.15 mmol) of tetrabutylammonium hydrogen sulfate in 100 ml of 60% potassium hydroxide solution/50 ml of toluene while being stirred vigorously at 0° C. It is stirred for 1 hour at 0° C. 200 ml of toluene is added, the aqueous phase is separated and extracted twice with 50 ml of toluene each. The combined organic phases are dried on magnesium sulfate and concentrated by evaporation in a vacuum. The residue is chromatographed on silica gel (mobile solvent: hexane/dichlormethane/acetone=20/10/1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06468502B1
Quelldatensatzuspto-grants-2002_10
ORD IDord-358a9c4b9de84f8795132100f5476ebc
Quellennotizuspto-grants-2002_10