Sodium Hydroxide → 2-Amino-5-chloro-2'-hydroxybenzophenone

HRID 1798

Reaktionsgleichung

Reaktionsgleichung von HRID 1798
C([NH:4][C:5]1[CH:20]=[CH:19][C:18]([Cl:21])=[CH:17][C:6]=1[C:7]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[O:15]C)=[O:8])(=O)C.[OH-].[Na+]>Br>[NH2:4][C:5]1[CH:20]=[CH:19][C:18]([Cl:21])=[CH:17][C:6]=1[C:7]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[OH:15])=[O:8]

Komponenten

4

Edukt 2

HCID 14798Sodium HydroxideHCID 12325888N-[4-Chloro-2-(2-methoxybenzoyl)phenyl]acetamide

Produkt 1

HCID 5264882-Amino-5-chloro-2'-hydroxybenzophenoneAusbeute 98,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 260Hydrogen BromideLösungsmittel

Versuchsvorschrift

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.

Aufarbeitung

  1. temperaturewas heated for 2 hours
  2. temperatureunder reflux
  3. extractionwas subjected to extraction with 200 ml of ethyl acetate
  4. washThe extract solution was washed with water
  5. dry with materialdried over anhydrous magnesium sulfate
  6. distillationthe solvent was then distilled off under reduced pressure
  7. customThe residue was purified by means of silica gel column chromatography (eluent, hexane:ethyl acetate=5:1)

Quellen und Nachweise

ORD-Eintrag
ord-64bedfb59dbe42709ee67ad4aa0bd72c
Quelldatensatz
uspto-grants-1998_03
Patentnummer
US05726306

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