تفاعل #531846

ord-2684c3753105439598e448632ab069ea

معادلة التفاعل

c1ccc(-n2c3ccccc3c3ccccc32)cc1
9-phenylcarbazole
O=C1CCC(=O)N1Br
N-bromosuccinimide
Cc1ccccc1
toluene
Brc1ccc2c(c1)c1ccccc1n2-c1ccccc1
3-bromo-9-phenyl-9H-carbazole
المردود 99.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىInto a 1000 mL three-neck flask were put
  2. 2
    غسيلThis suspending solution was washed with water, and magnesium sulfate
  3. 3
    workup.ADDITIONwas added
  4. 4
    أخرىso that moisture was removed
  5. 5
    ترشيحThen, the suspending solution was filtered
  6. 6
    أخرىto provide a filtrate
  7. 7
    أخرىwas obtained
  8. 8
    تركيزThe obtained filtrate was concentrated
  9. 9
    أخرىdried
  10. 10
    أخرىthe object of the synthesis
  11. 11
    أخرىwas obtained in a yield of 99% (synthesis scheme (a-6))

الإجراء التجريبي

Into a 1000 mL three-neck flask were put 24 g (100 mmol) of 9-phenylcarbazole, 18 g (100 mmol) of N-bromosuccinimide, 450 mL of toluene, and 200 mL of ethyl acetate, and the mixture was stirred for 45 hours at room temperature. This suspending solution was washed with water, and magnesium sulfate was added therein, so that moisture was removed. Then, the suspending solution was filtered to provide a filtrate was obtained. The obtained filtrate was concentrated and dried, whereby 32 g of a caramel-like solid of 3-bromo-9-phenyl-9H-carbazole, which was the object of the synthesis, was obtained in a yield of 99% (synthesis scheme (a-6)).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08475935B2uspto-grants-2013_07