Reaction #1528387

ord-4d78dc0764a84f049d0e1626a6b5e69c

Reaction equation

c1c[nH]cn1
imidazole
[K+].[OH-]
potassium hydroxide
BrCc1cccc(CBr)c1
α,α′-dibromo-m-xylene
c1cc(Cn2ccnc2)cc(Cn2ccnc2)c1
1-[3-(1H-imidazole-1yl-methyl)benzyl]-1H-imidazole
Yield 63.9%

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

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

Procedure

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

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07655323B2uspto-grants-2010_02