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HRID 2372105Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/2372105

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
Edukt2,3-Dichloro-1,1,1,4,4,4-hexafluorobut-2-eneHCID 9337—
Produkt2-Chloro-1,1,1,4,4,4-hexafluorobutaneHCID 273659641%

Reaktionsbedingungen

Temperatur250 °C

Reaktionsschritte

2,3-Dichlorohexafluorobut-2-ene (100 g) and iodine (55 g) were added to a 400 mL shaker tube. The tube was sealed, cooled, evacuated, and charged with 1500 psi of hydrogen at room temperature. The tube was then heated to 230° C. for 1 hour, 250° C. for 2 hours, and 260° C. for 15 hours. The tube was then cooled to room temperature, vented, and opened. The purple liquid was washed with water and then analyzed by GC/IR. Analysis of the washed liquid showed that it contained about 84% 2-chloro-1,1,1,4,4,4-hexafluorobutane, about 13% 2,3-dichloro-1,1,1,4,4,4-hexafluorobutane and about 1% 1,1,1,4,4,4-hexafluorobutane. The liquid was distilled on a concentric tube column yielding 35 g (41% isolated yield) of 2-chloro-1,1,1,4,4,4-hexafluorobutane (HCFC-346mdf) as a clear liquid with a b.p. of 50.9-51.4° C. 1H NMR (CHCl3 as internal standard): 4.4 ppm, complex, 1H; 2.9 ppm, complex, 1H; 2.7 ppm, complex, 1H. 19F NMR (CCl3F) as internal standard): 64.7 ppm, t, 1F; -76 ppm, d, 1F. GC/IR showed an identical spectrum to an authentic sample.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05097082
Quelldatensatzuspto-grants-1992_03
ORD IDord-3c7dfa0a7e954db78852163f254175c0
Quellennotizuspto-grants-1992_03