Реакция #79763

ord-55b7fb0c0aa44265ba7561577d290abe

Уравнение реакции

N#Cc1ccccc1F
2-fluorobenzonitrile
Oc1ccc(Br)cc1
4-bromophenol
O=C([O-])[O-].[K+].[K+]
potassium carbonate
N#Cc1ccccc1Oc1ccc(Br)cc1
2-(4-bromophenoxy)benzonitrile

Реагенты

Нет

Растворители

Условия реакции

Температура
120°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураwas heated
  2. 2
    workup.WAITto stand overnight at ambient temperature
  3. 3
    Другоеpartitioned between ethyl acetate and water
  4. 4
    ДругоеThe organic layer was separated
  5. 5
    Промывкаwashed
  6. 6
    Другоеdried
  7. 7
    Другоеevaporated
  8. 8
    Другоеto give an oil which
  9. 9
    ДругоеThe solid was triturated with petroleum ether b.p. 40-60° C.
  10. 10
    Фильтрацияfiltered

Методика

A mixture of 2-fluorobenzonitrile (28.8 g), 4-bromophenol (36.9 g), potassium carbonate (58.9 g) and dimethylformamide (30 ml) was heated with stirring under nitrogen at 120° C. for 5 hours. The mixture was allowed to stand overnight at ambient temperature and then partitioned between ethyl acetate and water. The organic layer was separated, washed, dried and evaporated to give an oil which solidified on standing. The solid was triturated with petroleum ether b.p. 40-60° C. and filtered to give 2-(4-bromophenoxy)benzonitrile.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06713474B2uspto-grants-2004_03