1-Bromohexane → 3-Hexylthiophene

HRID 863733ノート

反応式

HRID 863733 の反応式
Br[C:2]1[CH:6]=[CH:5][S:4][CH:3]=1.Br[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH3:13]>C(Cl)(Cl)Cl>[CH2:8]([C:2]1[CH:6]=[CH:5][S:4][CH:3]=1)[CH2:9][CH2:10][CH2:11][CH2:12][CH3:13]

参加物

4

実験手順

3-Hexylthiophene was synthesized by coupling the Grignard reagent of 3-bromothiophene with 1-bromohexane using bis(1,3-diphenylphosphino)propane nickel(II)chloride as catalyst. The product was purified by fractional distillation under reduced pressure. Polymerization of the monomer was achieved by mixing a 0.1M solution of 3-hexylthiophene in chloroform with a 0.4M chloroform solution of anhydrous ferric chloride. The mixture was stirred for two hours prior to precipitation into acidified methanol. The solid product was filtered, washed with NH4OH, water and methanol. The crude polymer was dissolved in hot dichloromethane and insoluble products were removed by filtration. Low molecular products were removed by cooling the filtrate and adding methanol. The precipitate was filtered and dried in a vacuum oven. The polymer possessed IR bands at 3027, 2930, 2859, 1458, 819, and 725 cm-1. The polymer had a number-average molecular weight of 9300 and a polydispersity index of 2.3.

後処理

  1. distillationThe product was purified by fractional distillation under reduced pressure
  2. customPolymerization of the monomer
  3. customto precipitation
  4. filtrationThe solid product was filtered
  5. washwashed with NH4OH, water and methanol
  6. dissolutionThe crude polymer was dissolved in hot dichloromethane
  7. custominsoluble products were removed by filtration
  8. customLow molecular products were removed
  9. temperatureby cooling the filtrate
  10. additionadding methanol
  11. filtrationThe precipitate was filtered
  12. customdried in a vacuum oven

出典と根拠

ORDレコード
ord-6a247e77c5514a39a40515f482036165
出典データセット
uspto-grants-1996_10
特許番号
US05561030

反応ノート

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