反応 #1994260

ord-a96a6ae6207e48c5a850b724648051a9

反応方程式

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
収率 70.0%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    洗浄the resultant solution was washed with distilled water
  2. 2
    抽出Then, an organic layer was extracted
  3. 3
    乾燥dried with sodium sulfate so as
  4. 4
    その他to remove the solvent
  5. 5
    その他The residue was purified by silica gel column chromatography (methylene chloride/n-hexane (1/10))

実験手順

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%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08597802B2uspto-grants-2013_12