反応 #1726663

ord-0f333ae6ef194d888e520232a8012227

反応方程式

O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
Ic1c2ccccc2c(-c2ccccc2)c2ccccc12
9-iodo-10-phenylanthracene
OB(O)c1ccc(-c2ccc(Br)cc2)cc1
4′-bromobiphenyl-4-boronic acid
Brc1ccc(-c2ccc(-c3c4ccccc4c(-c4ccccc4)c4ccccc34)cc2)cc1
light yellow powdered solid
収率 40.1%
Brc1ccc(-c2ccc(-c3c4ccccc4c(-c4ccccc4)c4ccccc34)cc2)cc1
9-(4′-bromobiphenyl-4-yl)-10-phenylanthracene
収率 40.1%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他Into a 100 mL three-neck flask were put
  2. 2
    その他to be degassed
  3. 3
    workup.STIRRINGThe mixture was stirred at 90° C. for 4 hours
  4. 4
    ろ過The mixture was subjected to suction filtration through alumina, Celite (produced by Wako Pure Chemical Industries, Ltd., Catalog No. 531-16855), and Florisil (produced by Wako Pure Chemical Industries, Ltd., Catalog No. 540-00135)
  5. 5
    その他The solid obtained by condensation of the obtained filtrate
  6. 6
    その他was purified by high-performance liquid chromatography (the mobile phase
  7. 7
    その他chloroform) to give a light yellow solid
  8. 8
    その他The obtained solid was recrystallized with chloroform/hexane

実験手順

Into a 100 mL three-neck flask were put 2.8 g (7.2 mmol) of 9-iodo-10-phenylanthracene and 1.5 g (7.2 mmol) of 4′-bromobiphenyl-4-boronic acid, and the atmosphere in the flask was replaced with nitrogen. To the mixture, 40 mL of toluene and 10 mL (2.0 mol/L) of a sodium carbonate aqueous solution were added. The mixture was stirred under reduced pressure to be degassed. After the degassing, 120 mg (0.10 mmol) of tetrakis(triphenylphosphine)palladium(0) was added to the mixture. The mixture was stirred at 90° C. for 4 hours. After the stirring, about 50 mL of toluene was added to the mixture. The mixture was subjected to suction filtration through alumina, Celite (produced by Wako Pure Chemical Industries, Ltd., Catalog No. 531-16855), and Florisil (produced by Wako Pure Chemical Industries, Ltd., Catalog No. 540-00135). The solid obtained by condensation of the obtained filtrate was purified by high-performance liquid chromatography (the mobile phase: chloroform) to give a light yellow solid. The obtained solid was recrystallized with chloroform/hexane to give 1.4 g of a light yellow powdered solid, which was the object of the synthesis, in a yield of 40%.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08110122B2uspto-grants-2012_02