Reaktion #79515

ord-33e013e936fb4fa9a30fbea89f8ede50

Reaktionsgleichung

O=N[O-].[Na+]
sodium nitrite
CCCCCCCCOc1cc2c3c(cccc3c1Sc1cccc(C)c1N)C(=O)c1ccccc1-2
3-[(2-amino-3-methylphenyl)thio]-2-octyloxy-7H-benzo[de]anthracene-7-one
CN(C)C=O
DMF
Cl
hydrochloric acid
CCCCCCCCOc1cc2c3ccccc3c(=O)c3ccc4c5c(C)cccc5sc1c4c32
6-n-Octyloxy-11-methyl-14H-anthra(2,1,9 mna)thioxanthene-14-one

Lösungsmittel

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeequipped with a mechanical stirrer
  2. 2
    SonstigeThe flask was set onto an ice bath
  3. 3
    Sonstigeexceeding 20° C
  4. 4
    workup.WAITheld for an hour
  5. 5
    Temperaturheated till 100° C
  6. 6
    Temperaturcooled
  7. 7
    Filtrationfiltered
  8. 8
    WaschenThe dark red colored precipitate was washed with ethanol and water
  9. 9
    SonstigeTm=207-209° C.

Vorschrift

70 g (0.14M) of 3-[(2-amino-3-methylphenyl)thio]-2-octyloxy-7H-benzo[de]anthracene-7-one and 1200 ml of DMF were placed into a 2 liter three-necked flask, equipped with a mechanical stirrer and a thermometer. The flask was set onto an ice bath. While stirring, 235 mg of 36% of hydrochloric acid has been added at a temperature not exceeding 20° C. After the reaction mixture was cooled to 0° C., 13.1 g of a sodium nitrite solution in 70 ml of water was added portionwise and held for an hour. Then 0.5 g of copper sulfate (II) has been added at 10° C. and heated till 100° C. The mixture was held for 2 hours, cooled and filtered. The dark red colored precipitate was washed with ethanol and water. The yield=60 g (89. Tm=207-209° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06713636B2uspto-grants-2004_03