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

HRID 248223

Reaction equation

HRID 248223 reaction equation
Cl[C:2](=[C:7]([Cl:12])[C:8]([F:11])([F:10])[F:9])[C:3]([F:6])([F:5])[F:4].II>>[Cl:12][CH:7]([CH2:2][C:3]([F:4])([F:5])[F:6])[C:8]([F:11])([F:10])[F:9]

Participants

3

Conditions

Temperature
250 °C

Procedure

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,l,1,4,4,4-hexafluorobutane (HCFC-346 mdf) 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, IH; 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.

Workup

  1. customThe tube was sealed
  2. temperaturecooled
  3. customevacuated
  4. additioncharged with 1500 psi of hydrogen at room temperature
  5. temperatureThe tube was then cooled to room temperature
  6. washThe purple liquid was washed with water
  7. distillationThe liquid was distilled on a concentric tube column

Sources & evidence

ORD record
ord-3ff1daa86afd43b8bad3de3a183b7528
Source dataset
uspto-grants-1993_05
Patent number
US05208396

Linked notes

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