Reaktion #92825

Reaktionsgleichung

2-iodo-9,10-diphenylanthracene

3-(dibenzothiophen-4-yl)-9H-carbazole

sodium tert-butoxide

tri(tert-butyl)phosphine

→

3-(dibenzothiophen-4-yl)-9-(9,10-diphenyl-2-anthryl)-9H-carbazole

Ausbeute 76.0%

Lösungsmittel

hexane

toluene

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeThis mixture was degassed
2. 2
   workup.STIRRINGThis mixture was stirred at 110° C. for 4 hours under a nitrogen stream
3. 3
   FiltrationAfter the stirring, the obtained mixture 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)
4. 4
   EinengenThe filtrate was concentrated
5. 5
   Sonstigeto give a yellow solid
6. 6
   SonstigeThe obtained solid was purified by silica gel column chromatography (developing solvent, hexane:toluene=5:1)
7. 7
   EinengenThe obtained fraction was concentrated
8. 8
   Sonstigeto give a yellow solid
9. 9
   SonstigeThe obtained yellow solid was recrystallized from toluene/hexane, so that 1.5 g of a yellow solid
10. 10
    Sonstigewas obtained in 76% yield
11. 11
    SonstigeThe synthesis scheme of Step 2

Vorschrift

To a 100-mL three-neck flask were added 1.4 g (3.0 mmol) of 2-iodo-9,10-diphenylanthracene, 1.1 g (3.0 mmol) of 3-(dibenzothiophen-4-yl)-9H-carbazole, and 0.86 g (9.0 mmol) of sodium tert-butoxide. After the air in the flask was replaced with nitrogen, to this mixture were added 20 mL of toluene and 0.2 mL of tri(tert-butyl)phosphine (a 10 wt % hexane solution). This mixture was degassed by being stirred while the pressure was reduced. After the degassing, 86 mg (0.15 mmol) of bis(dibenzylideneacetone)palladium(0) was added to the mixture. This mixture was stirred at 110° C. for 4 hours under a nitrogen stream. After the stirring, the obtained mixture 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). The filtrate was concentrated to give a yellow solid. The obtained solid was purified by silica gel column chromatography (developing solvent, hexane:toluene=5:1). The obtained fraction was concentrated to give a yellow solid. The obtained yellow solid was recrystallized from toluene/hexane, so that 1.5 g of a yellow solid was obtained in 76% yield. The synthesis scheme of Step 2 is illustrated in (b-7).

Quelle