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Ammonia → N-(4-iodophenyl)1,2-diaminobenzene

HRID 892755
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 892755
S(S([O-])=O)([O-])=O.[Na+].[Na+].[I:9][C:10]1[CH:15]=[CH:14][C:13]([NH:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=2[N+:23]([O-])=O)=[CH:12][CH:11]=1.N>O.C(O)C>[I:9][C:10]1[CH:15]=[CH:14][C:13]([NH:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=2[NH2:23])=[CH:12][CH:11]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 222AmmoniaHCID 24489Sodium DithioniteHCID 15045509N-(4-iodophenyl)-2-nitroaniline

Produkt 1

HCID 15045510N-(4-iodophenyl)1,2-diaminobenzene

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 702EthanolLösungsmittelHCID 962WaterLösungsmittel

Versuchsvorschrift

According to the method of Chem. Abs., 1962, 57, 9840a, a solution of sodium dithionite (85%, 24.74 g, 121 mmol) in water (120 ml) was added to a suspension of (4-iodophenyl)-2-nitroaniline in ethanol (500 ml). The mixture was heated under reflux for 45 minutes, cooled, treated with 300 ml of dilute aqueous ammonia, and concentrated under reduced pressure. The resulting white slurry was treated with 200 ml of dilute aqueous ammonia, filtered and washed with water (200 ml). The solid was dried in a vacuum desiccator at room temperature to give N-(4-iodophenyl)1,2-diaminobenzene, 8.91 g, which gradually darkens on exposure to light, m.p. 122°-123° C.

Aufarbeitung

  1. temperatureThe mixture was heated
  2. temperatureunder reflux for 45 minutes
  3. temperaturecooled
  4. concentrationconcentrated under reduced pressure
  5. additionThe resulting white slurry was treated with 200 ml of dilute aqueous ammonia
  6. filtrationfiltered
  7. washwashed with water (200 ml)
  8. customThe solid was dried in a vacuum desiccator at room temperature

Quellen und Nachweise

ORD-Eintrag
ord-f037d705155f4c70adc5e42c46f75a53
Quelldatensatz
uspto-grants-1992_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05120747

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