반응 #50900

ord-d30650a7d9c94a198aefea829969b8d9

반응 방정식

Nc1cccc2c(N)cccc12
1,5-Diaminonaphthalene
CC(C)(C)P(C(C)(C)C)C(C)(C)C
tri-t-butylphosphine
CC(C)(C)[O-].[Na+]
sodium t-butoxide
Brc1ccccc1
bromobenzene
c1ccc(Nc2cccc3c(N(c4ccccc4)c4ccccc4)cccc23)cc1
N,N,N′-triphenyl-1,5-diaminonaphthalene
수율 15.0%

용매

반응 조건

온도
140°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도After heating for another 6 h
  2. 2
    온도After heating for another 15 h the heat
  3. 3
    기타was removed
  4. 4
    온도After cooling to room temperature
  5. 5
    여과the solid present was filtered off
  6. 6
    기타the filtrate was purified by column chromatography

실험 절차

1,5-Diaminonaphthalene (16.0 g, 0.101 mol) was combined with bromobenzene (47.1 g, 0.300 mol), palladium diacetate (1.2 g, 0.004 mol), tri-t-butylphosphine (4 mL), sodium t-butoxide (24.0 g, 0.26 mol), and xylene (400 mL). The mixture was heated at 140° C. with magnetic stirring under a nitrogen atmosphere. After 15 h, an additional amount of palladium diacetate (0.100 g, 0.0004 mol) was added. After heating for another 6 h, an additional amount of palladium diacetate (0.100 g, 0.0004 mol) was added. After heating for another 15 h the heat was removed. After cooling to room temperature, the solid present was filtered off and the filtrate was purified by column chromatography. This afforded 6.0 g (15% yield) of N,N,N′-triphenyl-1,5-diaminonaphthalene.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06849345B2uspto-grants-2005_02