Реакция #43452

ord-5cffa760ea3a42c59d941a8a79d59029

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураThe reaction was refluxed for 18 h
  2. 2
    Концентрированиеconcentrated under reduced pressure
  3. 3
    ПромывкаThe residue was washed well with warm ethyl acetate
  4. 4
    КонцентрированиеThe combined ethyl acetate layer were concentrated
  5. 5
    Другоеdried
  6. 6
    ДругоеThe crude product was purified by flash column chromatography (silica gel, 4:1 and 2:1 hexane:ethyl acetate gradient)

Методика

To a solution of 7-bromo-2,3-dihydro-1-benzofuran-5-carbaldehyde (1.3 g, 4.7 mmol) in dimethylacetamide (2 mL) was added copper(I) cyanide (0.41 g g, 4.7 mmol). The reaction was refluxed for 18 h, and then concentrated under reduced pressure. The residue was washed well with warm ethyl acetate. The combined ethyl acetate layer were concentrated and dried. The crude product was purified by flash column chromatography (silica gel, 4:1 and 2:1 hexane:ethyl acetate gradient) to afford the desired product (0.5 g, 50%).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07732460B2uspto-grants-2010_06