4-Aminobenzoic Acid → HCID 86740683, Verbindung
Reaktionsgleichung
[NH2:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][CH:3]=1.[CH3:11][C:12]1([S:24]([O-:27])(=[O:26])=[O:25])[C:22](=[O:23])[C:21]2[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=2[C:14](=[O:15])[CH2:13]1.O.O.O.[Na+]>Cl>[CH3:11][C:12]1[C:22](=[O:23])[C:21]2[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=2[C:14](=[O:15])[CH:13]=1.[S:24](=[O:25])([OH:27])[O-:26].[NH2:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][CH:3]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 5 °C
Versuchsvorschrift
10 g of p-amino benzoic acid were dissolved in 65 g of an 8.5% aqueous solution of hydrochloric acid. To this solution, 25 g of powdery menadione sodium bisulfite was added. After this addition, the solution was cooled to 5° C.; a white precipitate was obtained, which, after filtering, washing and vacuum drying, weighed 24 g.
Aufarbeitung
- additionAfter this addition
- customa white precipitate was obtained
- filtrationwhich, after filtering
- washwashing
- customvacuum drying
Quellen und Nachweise
- ORD-Eintrag
- ord-ee65dd6a2bb34dd086c130fda93429b1
- Quelldatensatz
- uspto-grants-1986_03
- Patentnummer
- US04577019
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