Reaktion #92935

ord-213ef1a85db34e63bce76ce26da5f8f3

Reaktionsgleichung

Cc1ccc(C(=O)C(C)Br)cc1
1-(4-methylphenyl)-1-oxo-2-bromopropane
Cn1ccnc1
1-methylimidazole
Cc1ccc(C(=O)C(C)N2C=C[NH+](C)C2)cc1.[Br-]
1-methyl-3-[1-methyl-2-(4-methylphenyl)-2-oxoethyl]-1H-imidazolium bromide
Ausbeute 11.0%

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.DISSOLUTIONdissolved in acetonitrile
  4. 4
    workup.ADDITIONThe resulting solution was diluted with diethyl ether
  5. 5
    Filtrationthe precipitated solid was collected by filtration
  6. 6
    SonstigeThe solid was recrystallized from acetonitrile/diethyl ether

Vorschrift

A solution 2.24 g (0.01 mol) of 1-(4-methylphenyl)-1-oxo-2-bromopropane and 0.9 g (0.011 mol) of 1-methylimidazole in 50 ml of diethyl ether was stirred at room for approximately 18 hours. The reaction solvent was decanted, and the residue was washed with diethyl ether and dissolved in acetonitrile. The resulting solution was diluted with diethyl ether and the precipitated solid was collected by filtration. The solid was recrystallized from acetonitrile/diethyl ether to afford 0.33 g of 1-methyl-3-[1-methyl-2-(4-methylphenyl)-2-oxoethyl]-1H-imidazolium bromide as a solid. (11% yield) mp=175°-177° C.

Quelle

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