Реакция #577213

ord-f839fe5bb4354ca6ac278e5ae858b7ab

Уравнение реакции

N#Cc1ccc(-c2ccc(O)cc2)cc1
4-cyano-4′-hydroxybiphenyl
[Br-]
bromide
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CCC(C)=O
butanone
C=CCOc1ccc(-c2ccc(C#N)cc2)cc1
4-allyloxy-4′-cyanobiphenyl

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеA reaction mixture obtained
  2. 2
    Температураwas refluxed for 7 hours
  3. 3
    Другоеwas then separated
  4. 4
    ПромывкаAn organic layer was washed with water
  5. 5
    Сушкаdried over anhydrous magnesium sulfate
  6. 6
    workup.DISTILLATIONThe solvent was distilled off
  7. 7
    Другоеto obtain a residue, which
  8. 8
    Другоеwas purified by silica gel column chromatography
  9. 9
    Другоеsubjected to recrystallization from ethanol

Методика

A reaction mixture obtained by adding 20 g of 4-cyano-4′-hydroxybiphenyl, 20 g of ally bromide and 25 g of potassium carbonate to 250 mL of butanone was refluxed for 7 hours. Water was added to the reaction mixture, which was then separated. An organic layer was washed with water and dried over anhydrous magnesium sulfate. The solvent was distilled off to obtain a residue, which was purified by silica gel column chromatography using toluene as an elusion solvent and then subjected to recrystallization from ethanol to obtain 22 g of 4-allyloxy-4′-cyanobiphenyl.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07527746B2uspto-grants-2009_05