반응 #622417

ord-bf035b40aaba4cc38bb7e5d6d9711d46

반응 방정식

O=S([O-])([O-])=S.[Na+].[Na+]
sodium thiosulfate
c1ccc(-c2c3ccccc3cc3ccccc23)cc1
9-phenylanthracene
ClC(Cl)(Cl)Cl
carbon tetrachloride
ClC(Cl)(Cl)Cl
carbon tetrachloride
BrBr
bromine
Brc1c2ccccc2c(-c2ccccc2)c2ccccc12
9-bromo-10-phenylanthracene

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.WAITAfter a certain period
  2. 2
    workup.STIRRINGstirred for 1 hour
  3. 3
    추출an aqueous layer of the mixture was extracted with chloroform
  4. 4
    추출The obtained extracted solution
  5. 5
    세척washed with a 0.10 M sodium thiosulfate solution
  6. 6
    건조a saturated aqueous solution of sodium hydrogen carbonate, and saturated saline in this order, and then, the organic layer was dried with magnesium sulfate
  7. 7
    여과filtered
  8. 8
    기타condensed
  9. 9
    기타to give a solid
  10. 10
    여과A toluene solution of the solid was subjected to suction filtration through Celite (produced by Wako Pure Chemical Industries, Ltd., Catalog No. 531-16855), Florisil (produced by Wako Pure Chemical Industries, Ltd., Catalog No. 540-00135), and alumina
  11. 11
    기타condensed
  12. 12
    기타to give a solid
  13. 13
    기타this suspension was irradiated with ultrasonic waves
  14. 14
    기타was obtained by suction filtration in a yield of 84%

실험 절차

In a 300 mL three-neck flask, 5.8 g (23 mmol) of 9-phenylanthracene and 100 mL of carbon tetrachloride were placed. Then, 30 mL of a carbon tetrachloride solution containing 4.0 g (25 mmol) of bromine was dripped into the mixture under nitrogen stream. After dripping, the solution was stirred for 12 hours at room temperature. After a certain period, 100 mL of a 1.0 M sodium thiosulfate solution was added and stirred for 1 hour, and an aqueous layer of the mixture was extracted with chloroform. The obtained extracted solution and the organic layer were combined and washed with a 0.10 M sodium thiosulfate solution, a saturated aqueous solution of sodium hydrogen carbonate, and saturated saline in this order, and then, the organic layer was dried with magnesium sulfate. The mixture was gravity filtered, and the obtained filtrate was condensed to give a solid. A toluene solution of the solid was subjected to suction filtration through Celite (produced by Wako Pure Chemical Industries, Ltd., Catalog No. 531-16855), Florisil (produced by Wako Pure Chemical Industries, Ltd., Catalog No. 540-00135), and alumina, and the filtrate was condensed to give a solid. Methanol was added to the solid, and this suspension was irradiated with ultrasonic waves. Then, 6.4 g of a solid substance, which was target pale yellow powder, was obtained by suction filtration in a yield of 84%.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08859108B2uspto-grants-2014_10