Reaction #1994260

Reaction equation

10-(biphenyl-4-yl)-2-phenyl-9,10-dihydroacridine

bromosuccinimide

→

10-(biphenyl-4-yl)-2-bromo-7-phenyl-9,10-dihydroacridine

Yield 70.0%

Solvents

chloroform

Conditions

Workup

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

Procedure

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%).

Source