Reaktion #69529

ord-1febc6efb69144cd885e0f3d583c497d

Reaktionsgleichung

COc1cc(Br)cc(OC)c1
1-bromo-3,5-dimethoxybenzene
COc1cccc(OC)c1-c1ccccc1P(C1CCCCC1)C1CCCCC1
2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl
O=C([O-])[O-].[Cs+].[Cs+]
cesium carbonate
COc1cc(OC)cc(C2CC2)c1
title compound
COc1cc(OC)cc(C2CC2)c1
1-Cyclopropyl-3,5-dimethoxybenzene

Lösungsmittel

Reaktionsbedingungen

Temperatur
100°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionwas extracted with ethyl acetate
  2. 2
    Trocknendried over anhydrous magnesium sulfate
  3. 3
    workup.DISTILLATIONthe solvent was distilled off under reduced pressure
  4. 4
    SonstigeThe residue was purified by silica gel column chromatography (n-heptane/ethyl acetate: 3/1)

Vorschrift

To a solution of 1-bromo-3,5-dimethoxybenzene (2.00 g, 9.21 mmol) in dioxane (30 mL) and water (10 mL) were added potassium cyclopropyl trifluoroborate (2.73 g, 18.4 mmol), 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (756 mg, 1.84 mmol), palladium(II) acetate (207 mg, 0.92 mmol) and cesium carbonate (18.0 g, 55.3 mmol), and the mixture was heated at 100° C. for 16 hours. After the reaction was completed, water was added to the reaction mixture, which was extracted with ethyl acetate and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (n-heptane/ethyl acetate: 3/1) to obtain the title compound (1.61 g, 9.03 mmol).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08530504B2uspto-grants-2013_09