Реакция #1563944

ord-5800a0f975434b7d9fbbae5bc6d5d3e6

Растворители

Условия реакции

Температура
25°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.STIRRINGstirring
  2. 2
    workup.WAITwas continued at 100° C. for 3 h
  3. 3
    ТемператураThe reaction mixture was cooled to 25° C.
  4. 4
    Промывкаwashed with brine
  5. 5
    Сушкаdried over anhydrous sodium sulphate
  6. 6
    Концентрированиеconcentrated under reduced pressure
  7. 7
    Другоеto afford the crude, which
  8. 8
    Другоеwas purified by column chromatography (using silica gel and 2% ethyl acetate in Hexane as eluent)

Методика

To a solution of 3-bromo-5-fluorophenol (0.5 g, 2.6 mmol) in DMF (4.5 mL) was added K2CO3 (0.9 g, 6.54 mmol) and stirred at 25° C. for 10 min. Water (0.5 mL) was added to the above mixture followed by addition of 2-Chloro-2,2,-difluoroacetic acid sodium salt (0.6 g, 3.93 mmol) and stirring was continued at 100° C. for 3 h. The reaction mixture was cooled to 25° C. and diluted with ethyl acetate, washed with brine, dried over anhydrous sodium sulphate and concentrated under reduced pressure to afford the crude, which was purified by column chromatography (using silica gel and 2% ethyl acetate in Hexane as eluent) to afford the desired compound (Int-45). 1H NMR (400 MHz, CDCl3) δ ppm 7.2-6.9 (2H, m), 6.8-6.7 (1H, d), 6.7-6.2 (1H, m).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09402833B2uspto-grants-2016_08