4-Chloro-3-nitrobenzoic acid → 4-(Butylamino)-3-nitrobenzoic acid
Reaktionsgleichung
Cl[C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][C:3]=1[N+:11]([O-:13])=[O:12].[CH2:14]([NH2:18])[CH2:15][CH2:16][CH3:17]>>[CH2:14]([NH:18][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][C:3]=1[N+:11]([O-:13])=[O:12])[CH2:15][CH2:16][CH3:17]Komponenten
3
Versuchsvorschrift
A mixture of 50 parts of 4-chloro-3-nitrobenzoic acid and 222 parts of 1-butanamine was stirred for 3 hours at reflux temperature. After cooling and evaporation of the excess of 1-butanamine, the reaction mixture was acidified with a sulfuric acid solution 2N to pH 1. The precipitated product was filtered off and dried, yielding 59 parts (100%) of 4-(butylamino)-3-nitrobenzoic acid (int. 7).
Aufarbeitung
- temperatureat reflux temperature
- temperatureAfter cooling
- customevaporation of the excess of 1-butanamine
- filtrationThe precipitated product was filtered off
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-a2dfe26c41ef46dc9c3e07136e09ad8b
- Quelldatensatz
- uspto-grants-1991_08
- Patentnummer
- US05039677
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