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1,2-Dimethoxyethane → 1,2-Bis[2-methyl-5-(4-methyl-2-thienyl)-3-thienyl]hexafluorocyclopentene

HRID 3689
ノート
印刷プレビュー

反応式

HRID 3689 の反応式
Br[C:2]1[S:6][C:5]([CH3:7])=[C:4]([C:8]2[C:12]([F:14])([F:13])[C:11]([F:16])([F:15])[C:10]([F:18])([F:17])[C:9]=2[C:19]2[CH:23]=[C:22](Br)[S:21][C:20]=2[CH3:25])[CH:3]=1.[CH3:26][C:27]1[CH:28]=[C:29](OB(O)O)[S:30][CH:31]=1.C(=O)([O-])[O-].[K+].[K+].[CH2:42]([CH2:45]OC)OC>C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[Pd]>[CH3:25][C:20]1[S:21][C:22]([C:5]2[S:6][CH:2]=[C:42]([CH3:45])[CH:4]=2)=[CH:23][C:19]=1[C:9]1[C:10]([F:17])([F:18])[C:11]([F:15])([F:16])[C:12]([F:13])([F:14])[C:8]=1[C:4]1[CH:3]=[C:2]([C:29]2[S:30][CH:31]=[C:27]([CH3:26])[CH:28]=2)[S:6][C:5]=1[CH3:7]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 80711,2-DimethoxyethaneHCID 11430Potassium CarbonateHCID 149388943,3'-(Perfluorocyclopent-1-ene-1,2-diyl)bis(5-bromo-2-methylthiophene)HCID 544513244-Methyl-2-thienyl boric acid

生成物 1

HCID 189352461,2-Bis[2-methyl-5-(4-methyl-2-thienyl)-3-thienyl]hexafluorocyclopentene

試薬・触媒・溶媒 1

HCID 11979704
Tetrakis(triphenylphosphine)palladium
触媒

実験手順

1,2-Bis(5-bromo-2-methyl-3-thienyl)hexafluorocyclopentene (1.0 g 0.002 mol) was dissolved in dimethoxyethane (50 ml), and palladium tetra(triphenylphosphine) (120 mg) was added to the mixture which was stirred for 5 minutes under argon atmosphere. With 4-methyl-2-thienyl boric acid (852 mg, 0.006 mol) and an aqueous solution of potassium carbonate (0.1 mol dm-3, 10 ml) were added, the reaction mixture was refluxed for two hours. It was then concentrated under reduced pressures, extracted with diethylether and rinsed with water. With the diethylether removed under reduced pressures, the product was purified by alumina column chromatogram to give 1,2-bis[2-methyl-5-(4-methyl-2-thienyl)-3-thienyl]hexafluorocyclopentene (447 mg, 0.0008 mol).

後処理

  1. temperaturethe reaction mixture was refluxed for two hours
  2. concentrationIt was then concentrated under reduced pressures
  3. extractionextracted with diethylether
  4. washrinsed with water
  5. customWith the diethylether removed under reduced pressures
  6. customthe product was purified by alumina column chromatogram

出典と根拠

ORDレコード
ord-a4ed8d077a2e4b55a7f88a3b17be86f8
出典データセット
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05734065

反応ノート

読み込み中…

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