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

HRID 1199844Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1199844
[F:1][C:2]([F:11])([F:10])[C:3](Cl)=[CH:4][C:5]([F:8])([F:7])[F:6].[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

5

Versuchsvorschrift

40 g (0.2 mol) of 1,1,1,4,4,4-hexafluoro2-chloro-2-butene were hydrogenated in 300 ml of ethanol in the presence of 12 g of potassium hydroxide and 24 g of Raney nickel in the pressure range of from 20 to 40 bar and at a temperature from 20°to 100° C. The solid components were filtered off, the solvent was extracted with water, and the organic phase was separated and purified by distillation to give 15.5 g (47% of theory) of 1,1,1,4,4,4-hexafluorobutane. The boiling point was 25°to 27° C. at 1013 mbar.

Aufarbeitung

  1. filtrationThe solid components were filtered off
  2. extractionthe solvent was extracted with water
  3. customthe organic phase was separated
  4. distillationpurified by distillation

Quellen und Nachweise

ORD-Eintrag
ord-6292177f9c5e4a16a060a088c3cc2237
Quelldatensatz
uspto-grants-1990_02
Patentnummer
US04902839

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