2-Methyl-1-nitroanthraquinone → 1-Amino-2-methylanthraquinone

HRID 2072298

Reaktionsgleichung

Reaktionsgleichung von HRID 2072298
[N+:1]([C:4]1[C:17]2[C:16](=[O:18])[C:15]3[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=3)[C:9](=[O:19])[C:8]=2[CH:7]=[CH:6][C:5]=1[CH3:20])([O-])=O>O>[NH2:1][C:4]1[C:17]2[C:16](=[O:18])[C:15]3[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=3)[C:9](=[O:19])[C:8]=2[CH:7]=[CH:6][C:5]=1[CH3:20]

Komponenten

3

Edukt 1

HCID 314262-Methyl-1-nitroanthraquinone

Produkt 1

HCID 67021-Amino-2-methylanthraquinone

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

The wet filter cake of 1-nitro-2-methylanthraquinone (0.45 mole) was placed in a 5 l flask. To the flask was added 420 g (1.75 mole) of Na2S·9H2O dissolved in 2.5 l of H2O and the slurry was heated and then stirred at 95°-99° C for 2 hours. The reaction mixture was filtered and the orangish-red solid 1-amino-2-methylanthraquinone product was washed with hot H2O until the filtrate was clear and dried in vacuo at 70° C.

Aufarbeitung

  1. temperaturethe slurry was heated
  2. filtrationThe reaction mixture was filtered
  3. washthe orangish-red solid 1-amino-2-methylanthraquinone product was washed with hot H2O until the filtrate
  4. customdried in vacuo at 70° C.

Quellen und Nachweise

ORD-Eintrag
ord-57870156a21845989ba949d998cc881e
Quelldatensatz
uspto-grants-1977_09
Patentnummer
US04051138

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