Reaktion #1483123

ord-bd37c4f205544db2acadb02fb6b593e5

Reaktionsgleichung

c1ccc2cc(-c3cc4c5ccccc5c5ccccc5c4c4ccccc34)ccc2c1
10-(2-naphthyl)benzo[g]chrysene
BrBr
bromine
Brc1ccc2c(c1)c1ccccc1c1cc(-c3ccc4ccccc4c3)c3ccccc3c21
3-bromo-10-(2-naphthyl)benzo[g]chrysene
Ausbeute 90.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
100°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe resultant was heated
  2. 2
    TemperaturAfter cooling to room temperature
  3. 3
    SonstigeDeposited solids were separated by filtration
  4. 4
    Waschenwashed with water
  5. 5
    Trocknenwith methanol, and dried
  6. 6
    SonstigeThe thus obtained solids were purified by means of silica gel column chromatography

Vorschrift

4.05 g of 10-(2-naphthyl)benzo[g]chrysene and 400 mL of acetic acid were placed in a flask. 1.92 g of bromine was added, and the resultant was heated with stirring at 100° C. for 8 hours. After cooling to room temperature, the reaction solution was poured to 1 L of ice water. Deposited solids were separated by filtration, and washed with water and then with methanol, and dried. The thus obtained solids were purified by means of silica gel column chromatography, whereby 4.35 g (yield: 90%) of 3-bromo-10-(2-naphthyl)benzo[g]chrysene was obtained.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08900724B2uspto-grants-2014_12