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4-Aminophenol → Nitric Acid

HRID 377128
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 377128
[N+:1]([O-:4])([OH:3])=[O:2].C1C([NH2:11])=CC=C(O)C=1>>[N+:1]([O-:4])([O-:3])=[O:2].[OH:2][NH3+:1].[N+:1]([O-:4])([OH:3])=[O:2].[N+:1]([O-:4])([O-:3])=[O:2].[NH4+:11]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 4034-AminophenolHCID 944Nitric Acid4×

Produkt 3

HCID 944Nitric AcidHCID 22985Ammonium nitrateHCID 26045Hydroxylamine, nitrate

Versuchsvorschrift

The general procedure of Example 8 is repeated except that a solution containing 1.0 M nitric acid and 70 ppm p-aminophenol is charged to the catholyte compartment. A solution of 4 M nitric acid is charged to the anolyte compartment. Concentrated nitric acid is added to the catholyte compartment to maintain the nitric acid concentration between 0.5 M and 1 M under application of an electrical current. While maintaining the temperature between 5° C. and 10° C., a current of 20 amps (5 ASI) and a cell voltage of about 5 volts is applied. A solution of 1.26 M hydroxylammonium nitrate and 0.7 M nitric acid with no detectable ammonium nitrate is obtained from the catholyte compartment. An overall current efficiency of 74% for formation of hydroxylammonium nitrate is achieved.

Aufarbeitung

  1. additionis charged to the catholyte compartment
  2. temperatureWhile maintaining the temperature between 5° C. and 10° C.

Quellen und Nachweise

ORD-Eintrag
ord-3254ed99fb5344d4bc798d8824185458
Quelldatensatz
uspto-grants-2000_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06024855

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