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HRID 1443550Erstellt: 23. Oktober 2026

Hydrochloric Acid → 2-(4-Bromo-3-chloro-3,4,4-trifluorobutyl)-2-(2,2,3,4,4,4-hexafluorobutyl)malononitrile

https://huagongshe.com/de/reaction/1443550

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktPotassium CarbonateHCID 11430—
Edukt1,4-Dibromo-2-chloro-1,1,2-trifluorobutaneHCID 136221—
Edukt2-(2,2,3,4,4,4-Hexafluorobutyl)malononitrileHCID 86612538—
LösungsmittelDimethyl SulfoxideHCID 679—
Produkt2-(4-Bromo-3-chloro-3,4,4-trifluorobutyl)-2-(2,2,3,4,4,4-hexafluorobutyl)malononitrileHCID 866125376,3%

Reaktionsschritte

1.2 g of 2-(2,2,3,4,4,4-hexafluorobutyl)malononitrile and 1.5 g of 2-chloro-1,4-dibromo-1,1,2-trifluorobutane were dissolved in 10 ml of dimethyl sulfoxide, 0.7 g of potassium carbonate was added, and the mixture was stirred at room temperature for 5 hours. Thereafter, dilute hydrochloric acid was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layer was washed successively with water and aqueous saturated sodium chloride, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 0.14 g of 2-(4-bromo-3-chloro-3,4,4-trifluorobutyl)-2-(2,2,3,4,4,4-hexafluorobutyl)malononitrile (hereinafter, referred to as the present compound (46)).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07662402B2
Quelldatensatzuspto-grants-2010_02
ORD IDord-0975f7da5c10463f96adf96a25de6911
Quellennotizuspto-grants-2010_02