Réaction #1340566

ord-39532a2b992847c4ae3526acd742cae6

Équation de réaction

O=CC(=O)c1ccccc1
phenylglyoxal
Nc1c(N)c2ccccc2c2ccccc12
9,10-diaminophenanthrene
c1ccc(-c2cnc3c4ccccc4c4ccccc4c3n2)cc1
dibenzo[f,h]quinoxaline
Rendement 92.0%
c1ccc(-c2cnc3c4ccccc4c4ccccc4c3n2)cc1
2-Phenyldibenzo[f,h]quinoxaline
Rendement 92.0%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureThe solution was refluxed for 7 hours
  2. 2
    Autreto be reacted
  3. 3
    AutreThe white power precipitated through the reaction
  4. 4
    Filtrationwas filtered
  5. 5
    LavageThe residue was washed with ethanol

Mode opératoire

First, 2.16 g of phenylglyoxal and 3.36 g of 9,10-diaminophenanthrene were dissolved in a solvent of 100 mL of dehydrated ethanol under a nitrogen atmosphere. The solution was refluxed for 7 hours to be reacted. The white power precipitated through the reaction was filtered. The residue was washed with ethanol and then ether to give a dibenzo[f,h]quinoxaline derivative, Hdbq-P, which was the target substance (yield: 92%). Synthesis scheme of Step 1 is shown in (a-1) below.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08455111B2uspto-grants-2013_06