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

HRID 1460925

反応式

HRID 1460925 の反応式
[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]

参加物

3

反応条件

温度
-78 °C

実験手順

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, 1 F. 1HNMR (CHCl3 as internal standard): 5.27 ppm, dd, 1H; 3.55 ppm, c, 1H. The boiling point of this product was 67° C.

後処理

  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. washThe liquid was washed with water

出典と根拠

ORDレコード
ord-b385fcfdbca543d4b080793fc5518c86
出典データセット
uspto-grants-1991_12
特許番号
US05073288

関連ノート

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