Реакция #2876

ord-01265d1ee5214b12aaf7fb783abeb10c

Уравнение реакции

O=C1CCC(=O)N1Br
N-bromosuccinimide
OCc1cc(Br)ccc1F
5-bromo-2-fluoro-benzyl alcohol
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenyl phosphine
Fc1ccc(Br)cc1CBr
title compound
Выход 96.7%
Fc1ccc(Br)cc1CBr
5-Bromo-2-fluoro-benzyl bromide
Выход 96.7%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe ice bath is removed
  2. 2
    ДругоеThe crude product is purified by column chromatography
  3. 3
    Промывкаeluting with 5% EtOAc/hexanes

Методика

To a solution of 5-bromo-2-fluoro-benzyl alcohol (3.10 g, 15.1 mmol) in 30 mL of THF at 10° C. is added triphenyl phosphine (4.10 g, 15.6 mmol) followed by N-bromosuccinimide (2.67 g, 15.0 mmol). The ice bath is removed and the resulting solution is stirred for 20 min at room temperature. The crude product is purified by column chromatography eluting with 5% EtOAc/hexanes to give the title compound (3.90 g, 14.5 mmol).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05731315uspto-grants-1998_03