Reaktion #1895

ord-c2eabdf1be4f4a81a4b9a839ae6cea53

Reaktionsgleichung

Nc1ccc(Cl)cc1C(=O)c1ccccc1O
2-amino-5-chloro-2'-hydroxybenzophenone
O=C([O-])[O-].[K+].[K+]
potassium carbonate
BrCc1ccccc1
benzyl bromide
Nc1ccc(Cl)cc1C(=O)c1ccccc1OCc1ccccc1
2-amino-2'-benzyloxy-5-chlorobenzophenone

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    ExtraktionThe mixture was subjected to extraction with 150 ml of water and 200 ml of ethyl acetate
  2. 2
    Waschenthe ethyl acetate layer was washed with water
  3. 3
    Trocknendried over anhydrous magnesium sulfate
  4. 4
    workup.DISTILLATIONdistilled off under reduced pressure
  5. 5
    SonstigeThe residue was purified by means of silica gel column chromatography (eluent, hexane:ethyl acetate=10:1 to 5:1)

Vorschrift

In 30 ml of N,N-dimethylformamide was dissolved 5.0 g of 2-amino-5-chloro-2'-hydroxybenzophenone, as obtained in Example 123 (1), to which were added 4.2 g of potassium carbonate and 2.9 ml of benzyl bromide; the mixture was then stirred for 2 hours at room temperature. The mixture was subjected to extraction with 150 ml of water and 200 ml of ethyl acetate, and the ethyl acetate layer was washed with water, dried over anhydrous magnesium sulfate, and distilled off under reduced pressure. The residue was purified by means of silica gel column chromatography (eluent, hexane:ethyl acetate=10:1 to 5:1) to yield 6.4 g of 2-amino-2'-benzyloxy-5-chlorobenzophenone as prism crystals, m.p. 110° to 111° C.

Quelle

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