Réaction #1528387

Équation de réaction

imidazole

potassium hydroxide

α,α′-dibromo-m-xylene

→

1-[3-(1H-imidazole-1yl-methyl)benzyl]-1H-imidazole

Rendement 63.9%

Solvants

acetone

Conditions de réaction

Traitement

1. 1
   AutreTo a 500 mL round bottom flask equipped with a stirbar
2. 2
   FiltrationThe cloudy solution was filtered
3. 3
   Lavagethe white solids rinsed with acetone
4. 4
   AutreThe resulting filtrate was dried on silica
5. 5
   Autrepartitioned on a silica gel column
6. 6
   AutreThe product fractions were evaporated of solvent
7. 7
   Autrethe resulting oil recrystallized from ethyl acetate/hexanes

Mode opératoire

To a 500 mL round bottom flask equipped with a stirbar was added 11.6 g imidazole (170 mmol) and 9.55 g (170 mmol) finely pulverized potassium hydroxide. These were stirred in 200 mL acetone until the solution became yellow translucent. 15.0 g (56.8 mmol) α,α′-dibromo-m-xylene was then added, and the solution was stirred at room temperature overnight. The cloudy solution was filtered, and the white solids rinsed with acetone. The resulting filtrate was dried on silica and partitioned on a silica gel column using 30/70 acetonitrile/methanol as eluent. The product fractions were evaporated of solvent and the resulting oil recrystallized from ethyl acetate/hexanes to give 8.65 g 1-[3-(1H-imidazole-1yl-methyl)benzyl]-1H-imidazole as a white solid.

Source