تفاعل #1726663

ord-0f333ae6ef194d888e520232a8012227

معادلة التفاعل

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
المردود 40.1%
Brc1ccc(-c2ccc(-c3c4ccccc4c(-c4ccccc4)c4ccccc34)cc2)cc1
9-(4′-bromobiphenyl-4-yl)-10-phenylanthracene
المردود 40.1%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىInto a 100 mL three-neck flask were put
  2. 2
    أخرىto be degassed
  3. 3
    workup.STIRRINGThe mixture was stirred at 90° C. for 4 hours
  4. 4
    ترشيحThe 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
    أخرىThe solid obtained by condensation of the obtained filtrate
  6. 6
    أخرىwas purified by high-performance liquid chromatography (the mobile phase
  7. 7
    أخرىchloroform) to give a light yellow solid
  8. 8
    أخرىThe obtained solid was recrystallized with chloroform/hexane

الإجراء التجريبي

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%.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08110122B2uspto-grants-2012_02