Trifluoroacetic acid → HCID 178488964, Verbindung

HRID 275789

Reaktionsgleichung

Reaktionsgleichung von HRID 275789
[NH2:1][C:2]1[C:7]([NH2:8])=[CH:6][CH:5]=[CH:4][C:3]=1[O:9][CH3:10].[F:11][C:12]([F:17])([F:16])[C:13](O)=O>>[CH3:10][O:9][C:3]1[C:2]2[NH:1][C:13]([C:12]([F:17])([F:16])[F:11])=[N:8][C:7]=2[CH:6]=[CH:5][CH:4]=1

Komponenten

3

Versuchsvorschrift

A solution of 2,3-diaminoanisole (1.0 g) in trifluoroacetic acid (15 ml) was refluxed for 5 h and then stirred at room temperature overnight. Excess trifluoroacetic acid was removed in vacuo and the residue partitioned between ethyl acetate (50 ml) and water (50 ml). The organic phase was washed with saturated sodium bicarbonate solution (50 ml) and water (50 ml). Drying over anhydrous sodium sulfate and removal of the solvent in vacuo gave a brown residue. Purification by column chromatography eluting with 50% ethyl acetate in hexane gave the title compound as a yellow solid (1.4 g).

Aufarbeitung

  1. customExcess trifluoroacetic acid was removed in vacuo
  2. customthe residue partitioned between ethyl acetate (50 ml) and water (50 ml)
  3. washThe organic phase was washed with saturated sodium bicarbonate solution (50 ml) and water (50 ml)
  4. dry with materialDrying over anhydrous sodium sulfate and removal of the solvent in vacuo
  5. customgave a brown residue
  6. customPurification by column chromatography
  7. washeluting with 50% ethyl acetate in hexane

Quellen und Nachweise

ORD-Eintrag
ord-cd3646b14c6a4c6f81a7978aadde6c66
Quelldatensatz
uspto-grants-2002_03
Patentnummer
US06353010B1

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