Reaktion #1894

ord-64bedfb59dbe42709ee67ad4aa0bd72c

Reaktionsgleichung

COc1ccccc1C(=O)c1cc(Cl)ccc1NC(C)=O
2-acetylamino-5-chloro-2'-methoxybenzophenone
[Na+].[OH-]
sodium hydroxide
Nc1ccc(Cl)cc1C(=O)c1ccccc1O
2-amino-5-chloro-2'-hydroxybenzophenone
Ausbeute 98.1%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwas heated for 2 hours
  2. 2
    Temperaturunder reflux
  3. 3
    Extraktionwas subjected to extraction with 200 ml of ethyl acetate
  4. 4
    WaschenThe extract solution was washed with water
  5. 5
    Trocknendried over anhydrous magnesium sulfate
  6. 6
    workup.DISTILLATIONthe solvent was then distilled off under reduced pressure
  7. 7
    SonstigeThe residue was purified by means of silica gel column chromatography (eluent, hexane:ethyl acetate=5:1)

Vorschrift

A mixture of 10 g of 2-acetylamino-5-chloro-2'-methoxybenzophenone and 100 ml of 47% hydrogen bromide was heated for 2 hours under reflux. The solution was rendered neutral with sodium hydroxide, and was subjected to extraction with 200 ml of ethyl acetate. The extract solution was washed with water and dried over anhydrous magnesium sulfate; the solvent was then distilled off under reduced pressure. The residue was purified by means of silica gel column chromatography (eluent, hexane:ethyl acetate=5:1) to yield 8.0 g of 2-amino-5-chloro-2'-hydroxybenzophenone as needles.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05726306uspto-grants-1998_03