Reaktion #687335

Reaktionsgleichung

THF

9-bromo anthracene

p-tolylboronic acid

Na2CO3

→

white solid

Ausbeute 107.5%

9-p-tolyl-anthracene

Ausbeute 107.5%

Lösungsmittel

water

water

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.ADDITIONwere added into the flask
2. 2
   workup.ADDITIONwas added to the solution
3. 3
   Extraktionthe organic phase was extracted
4. 4
   SonstigeThe extracted organic phase was dried
5. 5
   Filtrationfiltered
6. 6
   Sonstigeto remove the solvent
7. 7
   workup.DISSOLUTIONThe dried organic phase was dissolved in a small amount of toluene
8. 8
   Sonstigeseparated
9. 9
   SonstigeA resulting solid was recrystallized

Vorschrift

5 g (1 eq, 15.6 mmol) of 9-bromo anthracene, 3.61 g of p-tolylboronic acid (1.7 eq, 26.5 mmol), 2.15 g (1.3 eq, 20.3 mmol) of Na2CO3, and 0.54 g (0.03 eq, 0.47 mmol) of tetrakis(triphenylphosphine)palladium were put into a 500-ml round-bottomed flask in Ar gas condition. 5 ml of THF and 2.2 ml of water, based on 1 mmol of p-tolylboronic acid, were added into the flask and refluxed at 85° C. for 16 hours. After the color of the solution changed to dark brown, water was added to the solution, and the organic phase was extracted using ethyl acetate. The extracted organic phase was dried using anhydrous magnesium sulfate and filtered to remove the solvent. The dried organic phase was dissolved in a small amount of toluene and separated using column chromatography (silica and hexane). A resulting solid was recrystallized using toluene and methanol to obtain 4.5 g (86%) of a white solid.

Quelle