Реакция #10166

ord-5ae0c0d393cb48bfbc9062688fae2658

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураThis mixture was heated
  2. 2
    Температураto reflux for 3.5 hours
  3. 3
    ДругоеThe solvent was then removed under reduced pressure
  4. 4
    ЭкстракцияThe organic layer was extracted with additional EtOAc
  5. 5
    ПромывкаThe combined organics were washed with water
  6. 6
    СушкаThe organics were then dried over sodium sulfate
  7. 7
    Фильтрацияfiltered
  8. 8
    Концентрированиеconcentrated
  9. 9
    Другоеto obtain the crude product
  10. 10
    Промывкаeluting with 8:1 heptane

Методика

To 500 mL of THF was added water (18.4 mL, 1.02 mol), potassium carbonate (70.5 g, 0.510 mol), methyl 2-iodobenzoate (53.5 g, 0.204 mol), 4-cyano-phenylboronic acid (30.0 g, 0.204 mol) and bis-(tri-o-tolylphosphine) palladium (II) chloride (1.65 g, 2.04 mmol). This mixture was heated to reflux for 3.5 hours and then cooled to ambient temperature for continued stirring overnight. The solvent was then removed under reduced pressure prior to dilution with EtOAc/water. The organic layer was extracted with additional EtOAc. The combined organics were washed with water, then brine. The organics were then dried over sodium sulfate, filtered, and then concentrated to obtain the crude product. This crude product was passed through a silica pad, eluting with 8:1 heptane:EtOAc to get 41.6 grams of methyl 4′-cyano-1,1′-biphenyl-2-carboxylate.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07091380B2uspto-grants-2006_08