Réaction #2069929

ord-d7eac201409d43deb09cba2b530eecf4

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreA solution prepared
  2. 2
    Températurewas refluxed for 7 hours
  3. 3
    Lavagethe organic layer was washed with water
  4. 4
    Séchagedried with anhydrous magnesium sulfate
  5. 5
    AutreThe solvent was evaporated away
  6. 6
    Autrethe resulting residue was purified through silica gel column chromatography
  7. 7
    Autrefurther recrystallized from ethanol

Mode opératoire

A solution prepared by adding 20 g of 4-cyano-4′-hydroxybiphenyl, 20 g of allyl bromide and 25 g of potassium carbonate to 250 ml of 2-butanone was refluxed for 7 hours. Water was added to the reaction solution for liquid-liquid separation, and the organic layer was washed with water and dried with anhydrous magnesium sulfate. The solvent was evaporated away, and the resulting residue was purified through silica gel column chromatography using toluene as an eluent solvent and then further recrystallized from ethanol to obtain 22 g of 4-allyloxy-4′-cyanobiphenyl.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07541071B2uspto-grants-2009_06