Methanol → Undecylenyl Iodide Eicosene

HRID 373756

反応式

HRID 373756 の反応式
[CH2:1]([I:12])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH:10]=[CH2:11].[CH2:13]=[CH:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32].[Cl-].C([Al+]CC)C.CO>C1(C)C=CC=CC=1>[CH2:1]([I:12])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH:10]=[CH2:11].[CH2:13]=[CH:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32]

参加物

6

反応条件

温度
25 °C

実験手順

To a glass screw top jar were added undecylenyl iodide (5 grams), toluene solvent (30 grams) and eicosene (5 grams, Aldrich Chemical). Under argon atmosphere were added diethyl aluminum chloride (10 milliliters of a 1.8 molar solution in toluene) and 0.5 teaspoon of TiCl3 --AA (available from Alfa, about 2 grams). Two additional charges of both catalysts were added in 90 minute intervals and then the reaction mixture was stirred for 16 hours at 25° C. Methanol was added and the mixture was precipitated into methanol/hydrochloric acid using a Waring blender. The solids were sequentially washed with methanol, water and then methanol using a blender and the residue was isolated by filtration and dried in vacuo to yield 6.26 grams of the grey rubbery product, poly(undecylenyl iodide-eicosene) copolymer. 13C NMR (in deuterated chloroform) analysis measured a ratio of CH2 --I groups to CH3 groups present to be 31 weight percent.

後処理

  1. additionTwo additional charges of both catalysts were added in 90 minute intervals
  2. customthe mixture was precipitated into methanol/hydrochloric acid using a Waring blender
  3. washThe solids were sequentially washed with methanol, water
  4. custommethanol using a blender and the residue was isolated by filtration
  5. customdried in vacuo

出典と根拠

ORDレコード
ord-73ac98c1423d472d898afb85def600b8
出典データセット
uspto-grants-1992_11
特許番号
US05166026

関連ノート

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