Reaktion #3114

ord-b2d252a75b1947e3893ae5090ef4d0e4

Reaktionsgleichung

O=[N+]([O-])c1ccc(O)cc1
4-Nitrophenol
O=C([O-])C(F)(F)Cl.[Na+]
sodium chlorodifluoroacetate
[Na+].[OH-]
sodium hydroxide
O=[N+]([O-])c1ccc(OC(F)F)cc1
title compound
Ausbeute 73.4%
O=[N+]([O-])c1ccc(OC(F)F)cc1
4-difluoromethoxynitrobenzene
Ausbeute 73.4%

Lösungsmittel

Reaktionsbedingungen

Temperatur
125°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe mixture was cooled to RT
  2. 2
    Extraktionwas extracted twice with ether
  3. 3
    WaschenThe combined organic extracts were washed twice with brine
  4. 4
    Trocknenwere dried (MgSO4)
  5. 5
    Filtrationfiltered
  6. 6
    Sonstigeevaporated
  7. 7
    SonstigeThe residue was purified by flash chromatography (silica gel, 25% ethyl acetate/hexanes )

Vorschrift

4-Nitrophenol (0.10 g, 0.72 mmol, Aldrich), sodium chlorodifluoroacetate (0.11 g, 0.72 mmol, Alfa Products) and sodium hydroxide (0.03 g, 0.72 mmol) were combined in dry DMF (1 mL) under an atmosphere of argon. After stirring at 125° C. for 1 h, the mixture was cooled to RT, was diluted with water and was extracted twice with ether. The combined organic extracts were washed twice with brine, were dried (MgSO4), filtered and evaporated. The residue was purified by flash chromatography (silica gel, 25% ethyl acetate/hexanes ) to provide the title compound as a white solid (0.10 g, 73%). mp 33°-35° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05731477uspto-grants-1998_03