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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199843Generated: October 25, 2026

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

https://huagongshe.com/reaction/1199843

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-1,1,1,4,4,4-hexafluoro-2-buteneHCID 9815—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
Product1,1,1,4,4,4-HexafluorobutaneHCID 6789047.8%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04902839
Source datasetuspto-grants-1990_02
ORD IDord-2050e1b3e6fa446d89c89f99ed642da0
Source noteuspto-grants-1990_02