Arsenic Acid → 4-Methyl-5,6-dimethoxy-8-nitroquinoline

HRID 1388559Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1388559
[CH3:1][O:2][C:3]1[C:9]([O:10][CH3:11])=[CH:8][C:6]([NH2:7])=[C:5]([N+:12]([O-:14])=[O:13])[CH:4]=1.[As](=O)(O)(O)O.P(=O)(O)(O)O.[CH:25]([C:27]([CH3:29])=O)=[CH2:26].C>>[CH3:11][O:10][C:9]1[C:3]([O:2][CH3:1])=[CH:4][C:5]([N+:12]([O-:14])=[O:13])=[C:6]2[C:8]=1[C:27]([CH3:29])=[CH:25][CH:26]=[N:7]2

Komponenten

6

Edukt 5

HCID 234Arsenic AcidHCID 297MethaneHCID 1004Phosphoric AcidHCID 6570Methyl vinyl ketoneHCID 46531524,5-Dimethoxy-2-nitroaniline

Produkt 1

HCID 6191084-Methyl-5,6-dimethoxy-8-nitroquinolineAusbeute 30 %

Versuchsvorschrift

A mixture of 4,5-dimethoxy-2-nitroaniline (3.96 g, 0.02 mol), arsenic acid (5.68 g, 0.04 mol) and 85% phosphoric acid (20 mL) was placed in a three-neck flask fitted with a thermometer and a dropping funnel. The reaction mixture was warmed to 100° (internal) with stirring and methyl vinyl ketone (2.1 g, 0.03 mol) was added at such a rate that the temperature was maintained at 100°±2°. After all the ketone was added, the mixture was stirred at 100° for an additional 30 min. The dark solution was poured into ice water (100 mL), treated with charcoal (Norit) and filtered. The filtrate was made alkaline (NH4OH) and extracted with chloroform. The extract was washed with water, dried (K2CO3), the solvent was evaporated and the dark residue was refluxed with benzene (100 mL). Insoluble tar was removed by filtration. The orange filtrate was concentrated to ca. 10 mL, placed on a silica gel column and eluted with benzene (ca. 2 L). The solvent was evaporated and the residue was recrystallized (×2) from methanol to give 1.3 g (30%) of the title compound, mp 123°-125°.

Aufarbeitung

  1. customwas placed in a three-neck flask
  2. customfitted with a thermometer and a dropping funnel
  3. temperatureThe reaction mixture was warmed to 100° (internal)
  4. temperaturewas maintained at 100°±2°
  5. stirringthe mixture was stirred at 100° for an additional 30 min
  6. filtrationfiltered
  7. extractionextracted with chloroform
  8. washThe extract was washed with water
  9. dry with materialdried (K2CO3)
  10. customthe solvent was evaporated
  11. temperaturethe dark residue was refluxed with benzene (100 mL)
  12. customInsoluble tar was removed by filtration
  13. concentrationThe orange filtrate was concentrated to ca. 10 mL
  14. washeluted with benzene (ca. 2 L)
  15. customThe solvent was evaporated
  16. customthe residue was recrystallized (×2) from methanol

Quellen und Nachweise

ORD-Eintrag
ord-71d9b14b55a84014a677c903d4a4c7e0
Quelldatensatz
uspto-grants-1984_02
Patentnummer
US04431807

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