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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372106Generated: October 25, 2026

Iodine → 2-Chloro-1,1,1,4,4,4-hexafluorobutane

https://huagongshe.com/reaction/2372106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant2,3-Dichloro-1,1,1,4,4,4-hexafluorobut-2-eneHCID 9337—
Product2-Chloro-1,1,1,4,4,4-hexafluorobutaneHCID 2736596—
Product2,3-Dichloro-1,1,1,4,4,4-hexafluorobutaneHCID 2774025—

Reaction Conditions

Temperature260 °C

Reaction Steps

2,3-Dichlorohexafluorobut-2-ene (300 g) and iodine (150 g) were charged into a 1 liter stirred autoclave. The autoclave was sealed, cooled and evacuated. It was then charged with hydrogen to 500 psi at room temperature. The autoclave was heated to 260° C. and the hydrogen pressure was increased to 1500 psi. The temperature was held at 260° C. with periodic additions of hydrogen to maintain a pressure of 1500 psi. After 15 hours no more hydrogen was being consumed by the reaction. The temperature was held for an additional six hours and then the clave was cooled and the gases were vented. The liquid was washed with water, saturated sodium thiosulfate solution, and then analyzed by GC/IR. Analysis showed that it contained 0.5% 1,1,1,4,4,4-hexafluorobutane, 85% 2-chloro-1,1,1,4,4,4-hexafluorobutane, and 13.5% of 2,3-dichloro-1,1,1,4,4,4-hexafluorobutane as two isomers. Distillation on a concentric tube column gave 78 g of 2-chloro-1,1,1,4,4,4-hexafluorobutane, and 25 g of 2,3-dichloro- 1,1,1,4,4,4-hexafluorobutane as two isomers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05097082
Source datasetuspto-grants-1992_03
ORD IDord-ab871f0846c64c96a4531978658d555d
Source noteuspto-grants-1992_03