Reaktion #93518

ord-d17fe45ddae24492a2764b6e70704cee

Reaktionsgleichung

CCCCn1ccnc1
1-butyl-1H-imidazole
COc1ccc(CCCBr)cc1
1-(3-bromopropyl)-4-methoxybenzene
CCCC[n+]1ccn(CCCc2ccc(OC)cc2)c1.[Br-]
title compound
CCCC[n+]1ccn(CCCc2ccc(OC)cc2)c1.[Br-]
1-Butyl-3-[3-(4-methoxyphenyl)propyl]imidazolium bromide

Reaktionsbedingungen

Temperatur
140°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe progress of the reaction by thin-layer chromatography on silica gel (methanol: 1M sodium chloride, 95:5)
  2. 2
    SonstigeAt the completion of the reaction
  3. 3
    Sonstigethe cooled reaction product
  4. 4
    Sonstigeis triturated thoroughly with ether
  5. 5
    Sonstigeon drying

Vorschrift

A mixture of 2.5 g (0.02 mole) of 1-butyl-1H-imidazole and 4.61 g (0.02 mole) of 1-(3-bromopropyl)-4-methoxybenzene is heated at 140° C. for about 1.5 hours. Follow the progress of the reaction by thin-layer chromatography on silica gel (methanol: 1M sodium chloride, 95:5). At the completion of the reaction, the cooled reaction product is triturated thoroughly with ether and on drying, provides the title compound.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04613609uspto-grants-1986_09