Reaktion #821338

ord-f8b246b3154d4837845e6b7c7370fe8d

Reaktionsgleichung

Cl.Cl.Nc1c(F)c(N)c(F)c(F)c1F
dihydrochloride
O=[N+]([O-])c1ccc(NC(CO)CO)cc1
2-(4-nitrophenylamino)propane-1,3-diol
→
Cl.Cl.Nc1ccc(NC(CO)CO)cc1
amine
Cl.Cl.Nc1ccc(NC(CO)CO)cc1
2-(4-aminophenylamino)propane-1,3-diol Dihydrochloride

Edukte

Cl.Cl.Nc1c(F)c(N)c(F)c(F)c1F
dihydrochloride
O=[N+]([O-])c1ccc(NC(CO)CO)cc1
2-(4-nitrophenylamino)propane-1,3-diol

Reagenzien

CCO.O.[Cl-].[NH4+].[Zn]
zinc ammonium chloride water ethanol

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

The 2-(4-nitrophenylamino)propane-1,3-diol (15) obtained above was reduced with a boiling zinc/ammonium chloride/water/ethanol mixture. The corresponding amine was isolated in dihydrochloride form.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07591860B2uspto-grants-2009_09