Potassium Carbonate → 1-(n-Octylsulfonylamino)-8-aminoanthraquinone

HRID 1087304

Reaktionsgleichung

Reaktionsgleichung von HRID 1087304
[NH2:1][C:2]1[C:15]2[C:14](=[O:16])[C:13]3[C:8](=[CH:9][CH:10]=[CH:11][C:12]=3Cl)[C:7](=[O:18])[C:6]=2[CH:5]=[CH:4][CH:3]=1.[CH3:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][S:27]([NH2:30])(=[O:29])=[O:28].C(=O)([O-])[O-].[K+].[K+]>ClC1C=CC=CC=1>[CH2:26]([S:27]([NH:30][C:12]1[C:13]2[C:14](=[O:16])[C:15]3[C:6](=[CH:5][CH:4]=[CH:3][C:2]=3[NH2:1])[C:7](=[O:18])[C:8]=2[CH:9]=[CH:10][CH:11]=1)(=[O:29])=[O:28])[CH2:25][CH2:24][CH2:23][CH2:22][CH2:21][CH2:20][CH3:19]

Komponenten

5

Edukt 3

HCID 11430Potassium CarbonateHCID 2236691-Amino-8-chloroanthraquinoneHCID 2295971-Octanesulfonamide

Produkt 1

HCID 198180061-(n-Octylsulfonylamino)-8-aminoanthraquinone

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 7964ChlorobenzeneLösungsmittel

Versuchsvorschrift

1-(n-octylsulfonylamino)-8-aminoanthraquinone was prepared as follows. 1-amino-8-chloroanthraquinone (1.0g), n-octanesulfonamide (1.0g), potassium carbonate (1.0g), cupric acetate monohydrate (0.85g) and chlorobenzene (16.0g) were refluxed for 5.5 hours. The cooled mixture was filtered and aqueous methanol was added to the filtrate. The supernatant liquid was decanted and the remaining oil was dissolved in dichloromethane. On addition of methanol and partial evaporation of the solvent, the product separated as a red solid.

Aufarbeitung

  1. filtrationThe cooled mixture was filtered
  2. additionaqueous methanol was added to the filtrate
  3. customThe supernatant liquid was decanted
  4. dissolutionthe remaining oil was dissolved in dichloromethane
  5. additionOn addition of methanol and partial evaporation of the solvent
  6. customthe product separated as a red solid

Quellen und Nachweise

ORD-Eintrag
ord-83651583e42e4f30a2ee99efb5716dee
Quelldatensatz
uspto-grants-1991_07
Patentnummer
US05034547

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