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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2106829Generated: 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/2106829

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-1,1,1,4,4,4-hexafluoro-2-buteneHCID 9815—
ReactantSodium HydroxideHCID 14798—
CatalystNickelHCID 935—
SolventDiglymeHCID 8150—
Product1,1,1,4,4,4-HexafluorobutaneHCID 6789075.3%

Reaction Steps

1,1,1,4,4,4-Hexafluoro-2-chloro-2-butene (199 g, 1 mole) in 800 ml diglyme was hydrogenated in the presence of sodium hydroxide (45 g) and Raney nickel (30 g) at a temperature of 20° to 40° 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 fractional distillation, giving 125 g (75% of theory) of 1,1,1,4,4,4-hexafluorobutane, boiling point 24°-27° C. at 1013 mbar. The 19F-nmr spectrum showed a resonance at -10.7 ppm (standard: CF3CO2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04931482
Source datasetuspto-grants-1990_06
ORD IDord-7cf76e483096422bb19b93593018cee4
Source noteuspto-grants-1990_06