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HRID 1031786Erstellt: 25. Oktober 2026

2-Chloro-1,1,1,4,4,4-hexafluoro-2-butene → 1,1,1,4,4,4-Hexafluorobutane

https://huagongshe.com/reaction/1031786

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Chloro-1,1,1,4,4,4-hexafluoro-2-buteneHCID 9815—
EduktPotassium HydroxideHCID 14797—
EduktHCID 178418361HCID 178418361—
KatalysatorNickelHCID 935—
LösungsmittelEthanolHCID 702—
Produkt1,1,1,4,4,4-HexafluorobutaneHCID 6789047,8%

Reaktionsschritte

In a stainless steel autoclave, 40 g of 1,1,1,4,4,4-hexafluoro-2-chloro-2-butene in 300 ml of ethanol were hydrogenated with hydrogen in the presence of 12 g of potassium hydroxide and 25 g of Raney nickel for 3 hours at 20° C. and another 1 hour at 100° C. at a pressure of from 30 to 40 bar. The solid components were then removed from the reaction mixture by filtration and the remaining liquid was distilled to give 16 g of 1,1,1,4,4,4-hexafluorobutane having a boiling point of 25-30° C. at 1013 mbar. The mass spectrum showed a molecular ion at m/e 166.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04954666
Quelldatensatzuspto-grants-1990_09
ORD IDord-a8edad7def86491a8bfd86f24820c110
Quellennotizuspto-grants-1990_09