Reaktion #78027

ord-70a34d2cf4ca4b2c893e159113b9d888

Reaktionsbedingungen

Temperatur
80°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeInto a separable flask equipped with a stirrer and a reflux condenser
  2. 2
    workup.ADDITIONwas added to the prepared solution
  3. 3
    TemperaturAfter the reaction solution was cooled to the room temperature
  4. 4
    Sonstigethe solid substance was removed by filtration
  5. 5
    EinengenThe filtrate was concentrated to about one half at a reduced pressure
  6. 6
    workup.ADDITIONTo the concentrated filtrate, 300 ml of water was added
  7. 7
    Sonstigethe formed solid substance was separated by filtration
  8. 8
    Sonstigeto obtain 2.9 g of a crude product
  9. 9
    SonstigeThe crude product was purified in accordance with the silica gel column chromatography

Vorschrift

Into a separable flask equipped with a stirrer and a reflux condenser cooled with water, 7.4 g of 3,3′-dinitro-4,4′-di-2-furoylaminobiphenyl, 100 ml of N-methyl-2-pyrrolidone and 75 ml of ethyl alcohol were placed. After adding 40 ml of a saturated aqueous solution of ammonium chloride, 25.6 g of powder of indium metal was added to the prepared solution. The obtained mixture was stirred at 80° C. for 1 hour. After the reaction solution was cooled to the room temperature, the solid substance was removed by filtration. The filtrate was concentrated to about one half at a reduced pressure. To the concentrated filtrate, 300 ml of water was added and the formed solid substance was separated by filtration to obtain 2.9 g of a crude product. The crude product was purified in accordance with the silica gel column chromatography to obtain 1.5 g of 3,3′-diamino-4,4′-di-2-furoylaminobiphenyl. The yield of the isolated product was 23%. This product was recrystallized from N-methyl-2-pyrrolidone/ethyl acetate (the volume ratio: 25/75) and needle crystals having a decomposition temperature of 256 to 259° C. were obtained.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06709804B2uspto-grants-2004_03