Reaktionsgleichung
[OH:1][C:2]1[N:6]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=2[N+:13]([O-])=O)[N:5]=[CH:4][C:3]=1[C:16]([O:18][CH2:19][CH3:20])=[O:17]>CO.[Pd]>[NH2:13][C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=1[N:6]1[C:2]([OH:1])=[C:3]([C:16]([O:18][CH2:19][CH3:20])=[O:17])[CH:4]=[N:5]1Komponenten
4
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
126.3 g of 5-hydroxy-1-(2-nitrophenyl)-1H-pyrazole-4-carboxylic acid, ethyl ester is dissolved in 1.6 liter methanol and 1.2 g Pd/C (10%) are added and hydrogenation is performed until H2 -uptake is finished (12 hours). After filtration the solvent is distilled off and the crystalline residue is recrystallized from dimethylformamide/ethanol to yield 78 g of 1-(2-aminophenyl)-5-hydroxy-1H-pyrazole-4-carboxylic acid, ethyl ester as white powder having a melting point of 151°-154° C.
Aufarbeitung
- custom(12 hours)
- filtrationAfter filtration the solvent
- distillationis distilled off
- customthe crystalline residue is recrystallized from dimethylformamide/ethanol
Quellen und Nachweise
- ORD-Eintrag
- ord-bc7311dbac1a4938810fb29dfe910d73
- Quelldatensatz
- uspto-grants-1981_04
- Patentnummer
- US04260751
Verknüpfte Notizen
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