Reaktion #1999473

ord-6be22cdf35f84ff5be69b61e7bd9083d

Reaktionsgleichung

O.O.[Cl][Sn][Cl]
Tin (II) chloride dihydrate
O=[N+]([O-])c1cc(F)c(Cl)cc1F
1-chloro-2,5-difluoro-4-nitrobenzene
O=C([O-])O.[Na+]
sodium bicarbonate
Nc1cc(F)c(Cl)cc1F
title compound
Ausbeute 73.9%
Nc1cc(F)c(Cl)cc1F
4-Chloro-2,5-difluorophenylamine
Ausbeute 73.9%

Lösungsmittel

Reaktionsbedingungen

Temperatur
70°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionextracted with ethyl acetate
  2. 2
    WaschenThe organic phase was washed several more times with water
  3. 3
    Sonstigedried
  4. 4
    Filtrationfiltered
  5. 5
    Einengenconcentrated
  6. 6
    Sonstigepurified by flash chromatography on silica gel (hexane/diethyl ether)

Vorschrift

Tin (II) chloride dihydrate (15.5 g, 68.7 mmol) was dissolved in ethyl acetate (50 mL) and 1-chloro-2,5-difluoro-4-nitrobenzene (2.65 g, 13.7 mmol) was added dropwise. The reaction mixture was then stirred at 70° C. for 1 h. The reaction mixture was then carefully added to saturated aqueous sodium bicarbonate and then extracted with ethyl acetate. The organic phase was washed several more times with water, dried, filtered, concentrated and purified by flash chromatography on silica gel (hexane/diethyl ether) to give the title compound as a white solid (1.65 g, 73.9% yield): 1H NMR (CDCl3): δ 7.02 (dd, 1H), 6.57 (dd, 1H), 3.81 (br s, 2H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08609592B2uspto-grants-2013_12