Reaktion #92933

ord-6430354e504d454496bcc68817c2b954

Reaktionsgleichung

Cc1ccccc1C(=O)CBr
1-bromo-2-(2-methylphenyl)-2-oxoethane
Cn1ccnc1
1-methylimidazole
Cc1ccccc1C(=O)CN1C=C[NH+](C)C1.[Br-]
1-methyl-3-[2-(2-methylphenyl)-2-oxoethyl]-1H-imidazolium bromide
Ausbeute 34.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe reaction solvent was decanted
  2. 2
    Waschenthe residue was washed with diethyl ether
  3. 3
    workup.DISSOLUTIONThe residue was dissolved in hot acetonitrile
  4. 4
    Temperaturthe resulting solution was cooled
  5. 5
    workup.ADDITIONdiluted with diethyl ether
  6. 6
    SonstigeThe solid was collected
  7. 7
    Sonstigerecrystallized twice from acetonitrile/diethyl ether

Vorschrift

A solution of 4.22 g (0.02 mol) of 1-bromo-2-(2-methylphenyl)-2-oxoethane, 2.64 g (0.032 mol) of 1-methylimidazole and 60 ml of diethyl ether was stirred at room temperature for approximately 17 hours. The reaction solvent was decanted and the residue was washed with diethyl ether. The residue was dissolved in hot acetonitrile, and the resulting solution was cooled and diluted with diethyl ether. The solid was collected and recrystallized twice from acetonitrile/diethyl ether to afford 1.99 g of 1-methyl-3-[2-(2-methylphenyl)-2-oxoethyl]-1H-imidazolium bromide as white needles. (34% yield) mp=152°-154° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04609670uspto-grants-1986_09