4-Aminobenzoic Acid → HCID 86740683, Verbindung

HRID 482969Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 482969
[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]=1

Komponenten

4

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

  1. additionAfter this addition
  2. customa white precipitate was obtained
  3. filtrationwhich, after filtering
  4. washwashing
  5. customvacuum drying

Quellen und Nachweise

ORD-Eintrag
ord-ee65dd6a2bb34dd086c130fda93429b1
Quelldatensatz
uspto-grants-1986_03
Patentnummer
US04577019

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