Реакция #92935

ord-213ef1a85db34e63bce76ce26da5f8f3

Уравнение реакции

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
Выход 11.0%

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe reaction solvent was decanted
  2. 2
    Промывкаthe 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
    Фильтрацияthe precipitated solid was collected by filtration
  6. 6
    ДругоеThe solid was recrystallized from acetonitrile/diethyl ether

Методика

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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04609670uspto-grants-1986_09