Potassium Carbonate → 9-[4-(Trifluoromethyl)phenyl]anthracene

HRID 1928973

反応式

HRID 1928973 の反応式
Br[C:2]1[C:3]2[C:8]([CH:9]=[C:10]3[C:15]=1[CH:14]=[CH:13][CH:12]=[CH:11]3)=[CH:7][CH:6]=[CH:5][CH:4]=2.[F:16][C:17]([F:28])([F:27])[C:18]1[CH:23]=[CH:22][C:21](B(O)O)=[CH:20][CH:19]=1.C1(C)C=CC=CC=1P(C1C=CC=CC=1C)C1C=CC=CC=1C.C(=O)([O-])[O-].[K+].[K+]>COCCOC>[F:16][C:17]([F:28])([F:27])[C:18]1[CH:23]=[CH:22][C:21]([C:2]2[C:3]3[C:8]([CH:9]=[C:10]4[C:15]=2[CH:14]=[CH:13][CH:12]=[CH:11]4)=[CH:7][CH:6]=[CH:5][CH:4]=3)=[CH:20][CH:19]=1

参加物

6

実験手順

5.1 g (20 mmol) of 9-bromoanthracene, 3.8 g (20 mmol) of 4-trifluoromethylphenylboronic acid, and 244 mg (0.8 mmol) of tri(o-tolyl)phosphine were put into a 100-mL three-neck flask, and nitrogen substitution in the system was carried out. 20 mL of ethylene glycol dimethyl ether (DME) was added to this mixture, and the mixture was stirred under reduced pressure and degassed. After that, 45 mg (0.20 mmol) of palladium acetate(II) and 10 mL (2.0 mol/L) of a potassium carbonate solution were added. This reaction mixture was stirred at 80° C. for 3 hours under nitrogen gas stream. Then, the reaction mixture was cooled to the room temperature, and a solid that was precipitated was collected by suction filtration. The collected solid was dissolved in toluene, and the solution was subjected to suction filtration through Florisil, celite, and then alumina. The filtrate was condensed to obtain a solid, and the solid was recrystallized with ethanol, whereby 5.7 g of a white powdery solid, which was a target matter, was obtained with the yield of 88%.

後処理

  1. customdegassed
  2. stirringThis reaction mixture was stirred at 80° C. for 3 hours under nitrogen gas stream
  3. customa solid that was precipitated
  4. filtrationwas collected by suction filtration
  5. dissolutionThe collected solid was dissolved in toluene
  6. filtrationthe solution was subjected to suction filtration through Florisil, celite
  7. customcondensed
  8. customto obtain a solid
  9. customthe solid was recrystallized with ethanol, whereby 5.7 g of a white powdery solid, which
  10. customwas obtained with the yield of 88%

出典と根拠

ORDレコード
ord-96fba1c7889646d8b748e68a0cdffc0b
出典データセット
uspto-grants-2012_05
特許番号
US08183793B2

関連ノート

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