Reaktion #679681

Reaktionsgleichung

7-(4-bromophenyl)-7H-dibenzo[c,g]carbazole

10-phenylanthracene-9-boronic acid

toluene

sodium carbonate

→

pale yellow powder

Ausbeute 55.0%

7-[4-(10-Phenyl-9-anthryl)phenyl]-7H-dibenzo[c,g]carbazole

Ausbeute 55.0%

Lösungsmittel

ethanol

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeIn a 200 mL three-neck flask were placed
2. 2
   SonstigeThis mixture was degassed
3. 3
   workup.STIRRINGthe mixture was stirred at 90° C. for 10 hours under a nitrogen stream
4. 4
   Sonstigeso that a solid was precipitated
5. 5
   SonstigeThe precipitated solid was removed by suction filtration
6. 6
   workup.DISSOLUTIONThe collected solid was dissolved in about 50 mL of hot toluene
7. 7
   Filtrationthis solution was suction-filtered through Celite (produced by Wako Pure Chemical Industries, Ltd., Catalog No. 531-16855), alumina, and Florisil (produced by Wako Pure Chemical Industries, Ltd., Catalog No. 540-00135)
8. 8
   SonstigeA solid obtained by concentration of the filtrate
9. 9
   Waschenwas washed with toluene/hexane

Vorschrift

In a 200 mL three-neck flask were placed 1.7 g (4.0 mmol) of 7-(4-bromophenyl)-7H-dibenzo[c,g]carbazole and 1.2 g (4.0 mmol) of 10-phenylanthracene-9-boronic acid, and the air in the flask was replaced with nitrogen. To this mixture were added 15 mL of toluene, 5.0 mL of ethanol, and 4.0 mL of an aqueous solution of sodium carbonate. This mixture was degassed by being stirred while the pressure was reduced. To this mixture was added 0.23 g (0.20 mmol) of tetrakis(triphenylphosphine)palladium(0), and the mixture was stirred at 90° C. for 10 hours under a nitrogen stream, so that a solid was precipitated. The precipitated solid was removed by suction filtration. The collected solid was dissolved in about 50 mL of hot toluene, and this solution was suction-filtered through Celite (produced by Wako Pure Chemical Industries, Ltd., Catalog No. 531-16855), alumina, and Florisil (produced by Wako Pure Chemical Industries, Ltd., Catalog No. 540-00135). A solid obtained by concentration of the filtrate was washed with toluene/hexane to give 1.3 g of a pale yellow powder, which was the object of the synthesis, in a yield of 55%. A synthesis scheme (d-2) of Step 4 is illustrated below.

Quelle