Реакция #57524

ord-e72283bc9ddc4e078eb8f910a1eef417

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураThe reaction mixture was refluxed for 6 h
  2. 2
    Фильтрацияfiltered
  3. 3
    КонцентрированиеThe filtrate was concentrated
  4. 4
    Другоеthe crude product was triturated with 10% EtOAc/hexane

Методика

To a solution of (6-bromo-3-methyl-benzofuran-2-yl)-(2,4-dichloro-phenyl)-methanone (3.0 g, 7.81 mmol) in carbon tetrachloride (30 mL) was added N-bromosuccinimide (1.46 g, 8.2 mmol) and 2,2′-azobisisobutyronitrile (128 mg, 0.78 mmol). The reaction mixture was refluxed for 6 h, then filtered. The filtrate was concentrated and the crude product was triturated with 10% EtOAc/hexane to afford the desired product as a pale yellow solid (2.85 g, 78.9%). This material was used in the subsequent step without further purification.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07420066B2uspto-grants-2008_09