Water → Methyl 3-amino-5-fluoro-2-nitrobenzoate
Reaktionsgleichung
[CH3:1][O:2][C:3](=[O:15])[C:4]1[CH:9]=[C:8]([F:10])[CH:7]=[C:6](F)[C:5]=1[N+:12]([O-:14])=[O:13].C(=O)([O-])[O-].[NH4+:20].[NH4+].O>CN(C=O)C>[CH3:1][O:2][C:3](=[O:15])[C:4]1[CH:9]=[C:8]([F:10])[CH:7]=[C:6]([NH2:20])[C:5]=1[N+:12]([O-:14])=[O:13]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 60 °C
Versuchsvorschrift
6.0 g (27.5 mmol) of 3,5-difluoro-2-nitro-benzoic acid methyl ester was dissolved in DMF and treated with 2.9 g (30.25 mmol) of ammonium carbonate. The reaction was heated at 60° C. for 6 h. Water was added to the reaction mixture. The solid produced was collected by filtration and washed with water to produce 3-amino-5-fluoro-2-nitro-benzoic acid methyl ester. LCMS: 215 (M+1)+.
Aufarbeitung
- customThe solid produced
- filtrationwas collected by filtration
- washwashed with water
Quellen und Nachweise
- ORD-Eintrag
- ord-47b33926b2d74870b937bae305ee0a1f
- Quelldatensatz
- uspto-grants-2013_12
- Patentnummer
- US08598353B2
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