ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

2,2'-Bithiophene → 5-Iodo-2,2'-bithiophene

HRID 1291581
ノート
印刷プレビュー

反応式

HRID 1291581 の反応式
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]1[S:7][CH:8]=[CH:9][CH:10]=1.[I:11]I.CCO>C(O)C>[I:11][C:5]1[S:1][C:2]([C:6]2[S:7][CH:8]=[CH:9][CH:10]=2)=[CH:3][CH:4]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 681202,2'-BithiopheneHCID 131719860I2 EtOH

生成物 1

HCID 113237785-Iodo-2,2'-bithiophene収率 186.1%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

33.2 g of 2,2'-bithiophene was dissolved in 50 ml of ethanol and I2 /EtOH (20.3 g/220 ml) was added. Then HIO3 /H2O (12 g/20 ml) were added slowly during 2 hours with stirring. The mixture was stirred for further 3 hours and the ethanol was evaporated. The residue was extracted with dichloromethane and dried over anhydrous magnesium sulfate. After the solvent was removed, the crude product was vacuum distilled to give 5-iodo-2,2'-bithiophene 36.8 g (105°-110° C./0.1 mm-Hg). The yield is 65-70%. The residue was purified by silica column chromatography and yielded 5.36 g of 5,5'-diiodo-2,2'-bithiophene (6.4%) with melting point of 170° C.

後処理

  1. stirringThe mixture was stirred for further 3 hours
  2. customthe ethanol was evaporated
  3. extractionThe residue was extracted with dichloromethane
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customAfter the solvent was removed
  6. distillationdistilled

出典と根拠

ORDレコード
ord-c6073b55a80b41dc91ed0fcf30645559
出典データセット
uspto-grants-1998_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05753692

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート