Réaction #302859

ord-62c22f3a95144fef8acb7e54e6623173

Équation de réaction

[Cl][Sn][Cl]
Tin(II) chloride
COc1ccc2oc(-c3ccc([N+](=O)[O-])cc3)cc(=O)c2c1
compound 23
COc1ccc2oc(-c3ccc([N+](=O)[O-])cc3)cc(=O)c2c1
6-methoxy-4′-nitroflavone
[Na+].[OH-]
sodium hydroxide
COc1ccc2oc(-c3ccc(N)cc3)cc(=O)c2c1
compound 24
COc1ccc2oc(-c3ccc(N)cc3)cc(=O)c2c1
6-methoxy-4′-aminoflavone

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureThe obtained mixture was heated
  2. 2
    Températureto reflux for 1 hour
  3. 3
    AutreAfter completion of the reaction
  4. 4
    Extractionthe obtained mixture was then extracted with 50 ml of ethyl acetate (150 ml)
  5. 5
    SéchageThe extract was dried over anhydrous sodium sulfate
  6. 6
    workup.DISTILLATIONthe solvent was then distilled away under reduced pressure

Mode opératoire

Tin(II) chloride (3.32 g, 17.5 mmol) was slowly added to an ethanol solution (30 ml) that contained compound 23 (520 mg, 1.75 mmol), while stirring. The obtained mixture was heated to reflux for 1 hour. After completion of the reaction, a 1 N sodium hydroxide aqueous solution (150 ml) was added to the reaction solution, and the obtained mixture was then extracted with 50 ml of ethyl acetate (150 ml). The extract was dried over anhydrous sodium sulfate, and the solvent was then distilled away under reduced pressure, so as to obtain a product of interest, 6-methoxy-4′-aminoflavone (compound 24) in the form of a yellow crystal. Yield: 360 mg (yield constant: 74.8%) 1H NMR (300 MHz, DMSO-d6) δ7.91 (d, J=8.7 Hz, 2H), 7.69-7.70 (m, 1H), 7.38-7.42 (m, 2H), 6.93 (d, J=9.0 Hz, 2H), 6.82 (s, 1H), 3.86 (s, 2H).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08192717B2uspto-grants-2012_06