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Trifluoroacetic acid → HCID 178488964, Verbindung

HRID 275789
Notizen
Druckvorschau

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
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 6422Trifluoroacetic acidHCID 1842683-Methoxybenzene-1,2-diamine

Produkt 1

HCID 178488964HCID 178488964, Verbindung

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. wash
The organic phase was washed with saturated sodium bicarbonate solution (50 ml) and water (50 ml)
  • dry with materialDrying over anhydrous sodium sulfate and removal of the solvent in vacuo
  • customgave a brown residue
  • customPurification by column chromatography
  • washeluting with 50% ethyl acetate in hexane
  • Quellen und Nachweise

    ORD-Eintrag
    ord-cd3646b14c6a4c6f81a7978aadde6c66
    Quelldatensatz
    uspto-grants-2002_03
    DOI
    10.6084/m9.figshare.5104873.v1
    Patentnummer
    US06353010B1

    Notizen zur Reaktion

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