Реакция #1722177

ord-62f78ef3c1a04108af31cf3e8034c25b

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураrefluxed for 2 hours
  2. 2
    Экстракцияextracted with ether
  3. 3
    Промывкаwashed with brine
  4. 4
    Сушкаdried over MgSO4
  5. 5
    Концентрированиеconcentrated

Методика

To a solution of 3-bromo-5-fluorobenzyl bromide (3.2 g, 0.0112 mole) in 1,4-dioxane (20 mL) was added a solution of KCN (0.82 g, 0.013 mole) in H2O (5 mL) and EtOH (5 mL), refluxed for 2 hours, extracted with ether, washed with brine, dried over MgSO4, and concentrated. Column chromatography was performed using hexane/ethyl acetate (19:1). 3-Bromo-5-fluorophenylacetonitrile was obtained was a colorless oil: 1H NMR (DMSO-d6) δ4.15 (s, 2H), 7.29(d, 1H, J=9.37 Hz), 7.47(s, 1H), 7.55(d, 1H, J=8.45 Hz); MS(EI) M+m/z 213; Anal. Calc. For C8H5BrFN: C, 44.89, H, 2.35, N,6.54. Found: C, 44.88, H, 2.32, N, 6.46.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06509334B1uspto-grants-2003_01