تفاعل #1980285

ord-da1f874af74444b19b1abdb3246d5ef8

معادلة التفاعل

c1ccc2c(c1)[nH]c1ccccc12
carbazole
Brc1ccc(Br)c2ccccc12
1,4-dibromonaphthalene
CCCCCC(N)N
diaminohexane
O=P([O-])([O-])[O-].[K+].[K+].[K+]
K3PO4
c1ccc(-c2ccc3[nH]c4ccc(-c5ccc(-c6cccc7ccccc67)cc5)cc4c3c2)cc1
title compound
المردود 6.0%
c1ccc(-c2ccc3[nH]c4ccc(-c5ccc(-c6cccc7ccccc67)cc5)cc4c3c2)cc1
4′-naphthyl-3,6-diphenylcarbazole
المردود 6.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىAs depicted in Reaction 6
  2. 2
    أخرىAfter completion of the reaction
  3. 3
    استخلاصthe reaction mixture was extracted with ethyl acetate
  4. 4
    أخرىAfter the solvent was removed under reduced pressure
  5. 5
    أخرىthe residue was purified by column chromatography

الإجراء التجريبي

As depicted in Reaction 6, a solution of 10 g (31.3 mmol) of carbazole, 13.5 g (31.3 mmol) of 1,4-dibromonaphthalene, CuI, diaminohexane and K3PO4 in dioxane was refluxed for 15 hours. After completion of the reaction, the reaction mixture was extracted with ethyl acetate. After the solvent was removed under reduced pressure, the residue was purified by column chromatography to give the title compound. The product was collected by filtration under reduced pressure and dried. Yield: 6%. MS (EI) (Calcd. for C34H22BrN: 523.09. Found: 523).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08512877B2uspto-grants-2013_08