Reaktion #1687951

ord-1eac948055264117a7adf9ef24ede3aa

Reaktionsgleichung

O=[N+]([O-])c1cc(F)c(Cl)cc1F
1-chloro-2,5-difluoro-4-nitrobenzene
NCC(=O)[O-].[Na+]
sodium glycinate
O=C([O-])CNc1cc(Cl)c(F)cc1[N+](=O)[O-].[Na+]
title compound
Ausbeute 64.0%
O=C([O-])CNc1cc(Cl)c(F)cc1[N+](=O)[O-].[Na+]
N-(5'-Chloro-4'-fluoro-2'-nitrophenyl)glycine sodium salt
Ausbeute 64.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe resulting suspension was refluxed for 60 h
  2. 2
    Filtrationthe precipitated bright orange solid was filtered
  3. 3
    Waschenwashed with cold ethanol (5 mL)
  4. 4
    Sonstigedried under vacuum

Vorschrift

To a stirred solution of 1-chloro-2,5-difluoro-4-nitrobenzene (0.825 g, 4.26 mmol) in ethanol (8.0 mL), was added a solution of sodium glycinate (0.415 g, 4.27 mmol) in water (1.5 mL). The resulting suspension was refluxed for 60 h. The solution was cooled to room temperature and the precipitated bright orange solid was filtered, washed with cold ethanol (5 mL), and dried under vacuum to give 0.673 g (64%) title compound as a bright orange powder; 1H NMR (DMSO-d6) δ 3.50 (d, 2H, J=3.6 Hz), 7.04 (d, 1H, J=6.6 Hz), 8.01 (d, 1H J=9.9 Hz), 8.74 (s, 1H). The unreacted 1-chloro-2,5-difluoro-4-nitrobenzene was recovered almost quantitatively from the filtrate.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05977107uspto-grants-1999_11