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

HRID 2372105

反応式

HRID 2372105 の反応式
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]

参加物

3

反応条件

温度
250 °C

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-3c7dfa0a7e954db78852163f254175c0
出典データセット
uspto-grants-1992_03
特許番号
US05097082

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