Reaktion #643393

ord-a099d0bb8de746cfae3aadfde3880673

Reaktionsgleichung

Brc1c2ccccc2cc2ccccc12
9-Bromoanthracene
OB(O)Oc1ccc2ccccc2c1
2-naphthyl boric acid
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
CCO
ethanol
c1ccc2cc(-c3c4ccccc4cc4ccccc34)ccc2c1
9-(2-naphthyl)anthracene

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturunder reflux for about 24 hours
  2. 2
    SonstigeThe organic layer was separated
  3. 3
    Waschenwashed with water
  4. 4
    Extraktionthe aqueous layer was extracted by chloroform
  5. 5
    ExtraktionThe organic extract
  6. 6
    Trocknenwas dried over magnesium sulfate
  7. 7
    Einengenconcentrated in vacuo
  8. 8
    Sonstigeto prepare

Vorschrift

9-Bromoanthracene (2.57 g, 10.00 mmol), 2-naphthyl boric acid (1.80 g, 12.65 mmol) and sodium carbonate (2.34 g, 22.1 mmol) were suspended in a mixture of toluene (20 mL), ethanol (3 mL) and water (10 mL). To the suspension, was added tetrakis(triphenylphosphine)palladium (0.25 g, 0.22 mmol). The mixture was stirred under reflux for about 24 hours, and then the refluxed mixture was cooled to room temperature. The organic layer was separated and washed with water, and the aqueous layer was extracted by chloroform. The organic extract was dried over magnesium sulfate, and concentrated in vacuo to prepare a 9-(2-naphthyl)anthracene compound C-1 (2.55 g, yield 84).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08053762B2uspto-grants-2011_11