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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2106831Generated: October 31, 2026

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

https://huagongshe.com/reaction/2106831

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-1,1,1,4,4,4-hexafluoro-2-buteneHCID 9815—
ReactantPotassium HydroxideHCID 14797—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
Product1,1,1,4,4,4-HexafluorobutaneHCID 6789047%

Reaction Steps

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

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04931482
Source datasetuspto-grants-1990_06
ORD IDord-dc030f493b004efa8ee0518ef191d7de
Source noteuspto-grants-1990_06