Reaktion #95042

ord-d12c6c991ea148f29868549018fcf0e6

Reaktionsgleichung

O=[N+]([O-])c1cccc(O)c1
3-nitrophenol
N#CCCl
chloroacetonitrile
O=C([O-])[O-].[K+].[K+]
K2CO3
O
water
N#CCOc1cccc([N+](=O)[O-])c1
3-nitrophenoxyacetonitrile
Ausbeute 88.0%

Lösungsmittel

Reaktionsbedingungen

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

Aufarbeitung

  1. 1
    Temperaturwas heated
  2. 2
    Sonstigeresulted in crystal formation
  3. 3
    Filtrationthe solids were filtered
  4. 4
    Waschenwashed well with water
  5. 5
    Sonstigedried overnight in a vacuum oven
  6. 6
    workup.ADDITIONtreated with activated charcoal
  7. 7
    Filtrationfiltered
  8. 8
    Sonstigethe resulting solids removed by filtration
  9. 9
    SonstigeDrying in a vacuum oven

Vorschrift

A mixture of 41.7 grams (g) of 3-nitrophenol, 24 g of chloroacetonitrile and 58.8 g of anhydrous K2CO3 in 60 milliliters (ml) of DMSO was heated with stirring in a round-bottomed three-necked flask at 70°-80° C. for 3 hours. The reaction mixture was then poured into 1200 ml of ice and water, which resulted in crystal formation. When all of the ice had melted, the solids were filtered, washed well with water and dried overnight in a vacuum oven. The solids were then put in solution in 400 ml of boiling absolute ethanol, treated with activated charcoal and then filtered. The filtrate was cooled to 0° C. and the resulting solids removed by filtration. Drying in a vacuum oven gave 47 g of 3-nitrophenoxyacetonitrile as a pale tan solid having a melting point (m.p.) of 93°-95° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04343808uspto-grants-1982_08