반응 #1801595

ord-748c9982337847febbb61fbfb780f691

반응 방정식

c1ccc(-c2c3ccccc3cc3ccccc23)cc1
9-phenylanthracene
BrBr
bromine
O=S([O-])([O-])=S.[Na+].[Na+]
sodium thiosulfate
Brc1c2ccccc2c(-c2ccccc2)c2ccccc12
10-bromo-9-phenylanthracene
수율 99.6%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONwas dropped into the reaction solution
  2. 2
    기타After the reaction
  3. 3
    기타the reaction
  4. 4
    세척An organic layer was washed with an aqueous sodium hydroxide (NaOH) solution
  5. 5
    건조a saturated sodium chloride solution and dried with magnesium sulfate
  6. 6
    여과The mixture was naturally filtered
  7. 7
    기타a compound obtained
  8. 8
    농축by concentrating the filtrate
  9. 9
    workup.DISSOLUTIONwas dissolved into toluene
  10. 10
    여과filtered through florisil, Celite®, and alumina
  11. 11
    농축The filtrate was concentrated
  12. 12
    기타recrystallized with dichloromethane and hexane

실험 절차

6.0 g (23.7 mmol) of 9-phenylanthracene was dissolved into 80 mL of carbon tetrachloride, and a solution in which 3.80 g (21.1 mmol) of bromine was dissolved in 10 mL of carbon tetrachloride was dropped into the reaction solution using a dropping funnel. After dropping, the solution was stirred for 1 hour at a room temperature. After the reaction, an aqueous sodium thiosulfate solution was added to stop the reaction. An organic layer was washed with an aqueous sodium hydroxide (NaOH) solution and a saturated sodium chloride solution and dried with magnesium sulfate. The mixture was naturally filtered, and a compound obtained by concentrating the filtrate was dissolved into toluene and filtered through florisil, Celite®, and alumina. The filtrate was concentrated and recrystallized with dichloromethane and hexane, thereby obtaining 7.0 g of objective 10-bromo-9-phenylanthracene as a light-yellow solid with a yield of 89%.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07795449B2uspto-grants-2010_09