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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 396597Erstellt: 24. Oktober 2026

Dimethyl Sulfate → Methyl perfluorobutyl ether

https://huagongshe.com/de/reaction/396597

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfateHCID 6497—
EduktCesium fluorideHCID 25953—
EduktDecafluorocyclohexanoneHCID 12570757—
LösungsmittelWaterHCID 962—
LösungsmittelDiglymeHCID 8150—
ProduktMethyl perfluorobutyl etherHCID 164514—

Reaktionsschritte

A 500 ml, 3-necked round bottom flask equipped with an overhead stirrer, an addition funnel, and a condenser was charged with anhydrous cesium fluoride (27.4 g, 0.18 mole), anhydrous diethylene glycol dimethyl ether (258 g, hereinafter diglyme), and dimethyl sulfate (22.7 g, 0.18 mole). Perfluorocyclohexanone (50 g, 0.18 mole) was then added dropwise to the resulting stirred mixture, and stirring was continued for 18 hours after the addition. Water (approximately 200 ml) was added to the resulting mixture, and the lower fluorochemical phase of the mixture was separated from the upper phase and washed once with saturated aqueous sodium chloride solution. Since the fluorochemical phase still contained about 12% diglyme, water was added to it, and the resulting product was azeotropically distilled to yield 32.8 g of c-C6F11OCH3 (b.p.=100° C.), which was free of diglyme. The product identity was confirmed by IR, GCMS, and 1H and 19F NMR.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06608019B1
Quelldatensatzuspto-grants-2003_08
ORD IDord-a36f776f5c0d49f6bc46991601580948
Quellennotizuspto-grants-2003_08