Reaktion #1747844

ord-63e0eabc98a344d391807e2e96190728

Reaktionsgleichung

OB(O)c1cc2ccccc2c2ccccc12
9-phenanthreneboronic acid
Brc1cccc(I)c1
3-bromoiodobenzene
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
Brc1cccc(-c2cc3ccccc3c3ccccc23)c1
9-(3-bromophenyl)phenanthrene
Ausbeute 74.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwhile being refluxed
  2. 2
    SonstigeAfter the reaction
  3. 3
    TrocknenAfter organic phase thereof was dried with magnesium sulfate
  4. 4
    workup.DISTILLATIONthe toluene was distilled away under reduced pressure
  5. 5
    Sonstigewas obtained with an yield of 74%

Vorschrift

Under an argon gas atmosphere, 31.4 g (141 mmol) of 9-phenanthreneboronic acid, 40.0 g (141 mmol) of 3-bromoiodobenzene, 3.30 g (2.83 mmol) of tetrakis(triphenylphosphine) palladium(0), 200 mL of toluene, 50 mL of dimethoxyethane and 212 mL of 2M sodium carbonate solution were mixed, and stirred for four hours while being refluxed. After the reaction, the reaction mixture was further added with toluene, and cleansed by water. After organic phase thereof was dried with magnesium sulfate, the toluene was distilled away under reduced pressure. Residue thereof was refined by silica-gel column chromatography, such that 34.7 g of 9-(3-bromophenyl)phenanthrene was obtained with an yield of 74%.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08029697B2uspto-grants-2011_10