Реакция #66035

ord-0d65275dc5704080bbbbe2b39cde242f

Уравнение реакции

O
water
c1ccc2c(c1)[nH]c1ccccc12
carbazole
CC(=O)c1ccc(F)cc1
4-fluoroacetophenone
O=C([O-])[O-].[K+].[K+]
K2CO3
CC(=O)c1ccc(-n2c3ccccc3c3ccccc32)cc1
product
CC(=O)c1ccc(-n2c3ccccc3c3ccccc32)cc1
1-(4-Carbazol-9-yl-phenyl)ethanone

Реагенты

Нет

Растворители

Условия реакции

Температура
135°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеto afford a precipitate
  2. 2
    Другоеwhich is isolated by filtration
  3. 3
    Промывкаwashed with water
  4. 4
    ДругоеThe crude product thus obtained
  5. 5
    Другоеis further purified by recrystallization from TBME (tert-butyl methyl ether)

Методика

To carbazole (5.02 g) in DMSO (50 mL) is added 4-fluoroacetophenone (3.45 g) and K2CO3 (10.4 g), and the mixture is stirred at 135° C. overnight. The mixture is poured into water to afford a precipitate, which is isolated by filtration and washed with water. The crude product thus obtained is further purified by recrystallization from TBME (tert-butyl methyl ether), giving the product as a light brown solid. The structure is confirmed by the 1H-NMR spectrum (CDCl3). δ [ppm]: 2.71 (s, 3H), 7.32 (ddd, 2H), 7.41-7.50 (m, 4H), 7.72 (d, 2H), 8.15 (d, 2H), 8.21 (d, 2H).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08524425B2uspto-grants-2013_09