Reaktion #1994260

ord-a96a6ae6207e48c5a850b724648051a9

Reaktionsgleichung

c1ccc(-c2ccc(N3c4ccccc4Cc4cc(-c5ccccc5)ccc43)cc2)cc1
10-(biphenyl-4-yl)-2-phenyl-9,10-dihydroacridine
O=C1CC(Br)C(=O)N1
bromosuccinimide
Brc1ccc2c(c1)Cc1cc(-c3ccccc3)ccc1N2c1ccc(-c2ccccc2)cc1
10-(biphenyl-4-yl)-2-bromo-7-phenyl-9,10-dihydroacridine
Ausbeute 70.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Waschenthe resultant solution was washed with distilled water
  2. 2
    ExtraktionThen, an organic layer was extracted
  3. 3
    Trocknendried with sodium sulfate so as
  4. 4
    Sonstigeto remove the solvent
  5. 5
    SonstigeThe residue was purified by silica gel column chromatography (methylene chloride/n-hexane (1/10))

Vorschrift

10-(biphenyl-4-yl)-2-phenyl-9,10-dihydroacridine (7.8 g, 19.0 mmol) was added with chloroform (300 ml), and with bromosuccinimide (3.7 g, 21.0 mmol). The resultant solution was stirred at room temperature for 2 hours. After the reaction was completed, the resultant solution was washed with distilled water. Then, an organic layer was extracted and dried with sodium sulfate so as to remove the solvent. The residue was purified by silica gel column chromatography (methylene chloride/n-hexane (1/10)) to obtain 10-(biphenyl-4-yl)-2-bromo-7-phenyl-9,10-dihydroacridine compound (pale yellow solid, 6.5 g, yield 70%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08597802B2uspto-grants-2013_12