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

HRID 1031786Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1031786
[F:1][C:2]([F:11])([F:10])[C:3](Cl)=[CH:4][C:5]([F:8])([F:7])[F:6].[H][H].[OH-].[K+]>C(O)C.[Ni]>[F:1][C:2]([F:11])([F:10])[CH2:3][CH2:4][C:5]([F:8])([F:7])[F:6]

Komponenten

6

Versuchsvorschrift

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.

Aufarbeitung

  1. customThe solid components were then removed from the reaction mixture by filtration
  2. distillationthe remaining liquid was distilled

Quellen und Nachweise

ORD-Eintrag
ord-a8edad7def86491a8bfd86f24820c110
Quelldatensatz
uspto-grants-1990_09
Patentnummer
US04954666

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