Iodine → 1,1,1,2,2,3,5,5,5-Nonafluoro-4-(trifluoromethyl)pentane

HRID 1461679

Reaktionsgleichung

Reaktionsgleichung von HRID 1461679
[F:1][C:2]([F:18])([F:17])[C:3]([C:13]([F:16])([F:15])[F:14])=[C:4]([F:12])[C:5]([F:11])([F:10])[C:6]([F:9])([F:8])[F:7].II>>[F:7][C:6]([F:8])([F:9])[C:5]([F:10])([F:11])[CH:4]([F:12])[CH:3]([C:13]([F:15])([F:14])[F:16])[C:2]([F:18])([F:17])[F:1]

Komponenten

3

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

Perfluoro-2-methylpent-2-ene (3 g) and iodine (1.25 g) were sealed in a 10 mL pressure tube. The tube was cooled to -78° C., evacuated, and charged with 1500 psi of hydrogen at room temperature. The tube was then heated at 240° C. for 1 h, and 260° C. for 15 h. The tube was cooled, vented, and opened The liquid was washed with water, giving 1,1,1,2,2,3,5,5,5-nonafluoro-4-trifluoromethylpentane (1.38 g) which was 99.5% pure by GC analysis GC/IR 3000 cm-1, w (C-H); 1288 cm-1 , vs (C-F); 1228 cm-1, vs (C-F); 691 cm-1, m. 19FNMR (CCl3F as internal standard): -62 ppm, c, 3F; -67 5 ppm, c, 3F; -83.9 ppm, t, 3F; -122-133 ppm, AB, 2F; -212.2 ppm, c, 1F. 1HNMR (CHCl3 as internal standard): 5.27 ppm, dd, 1H; 3.55 ppm, c, 1H. The boiling point of this product was 67° C.

Aufarbeitung

  1. customevacuated
  2. additioncharged with 1500 psi of hydrogen at room temperature
  3. temperatureThe tube was then heated at 240° C. for 1 h
  4. temperatureThe tube was cooled
  5. washwas washed with water

Quellen und Nachweise

ORD-Eintrag
ord-3b322ee72dd2436eb9bdb5eae82b7528
Quelldatensatz
uspto-grants-1991_12
Patentnummer
US05076956

Verknüpfte Notizen

Wird geladen…