Réaction #59025

ord-f2916d53218449efbbc1f71d07798d98

Équation de réaction

O
Water
CCOC(=O)CBr
Ethyl bromoacetate
CC(=O)c1cc(Br)ccc1O
5-bromo-2-hydroxyacetophenone
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CCOC(=O)COc1ccc(Br)cc1C(C)=O
ethyl (2-acetyl-4-bromophenoxy)acetate

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.STIRRINGthe mixture was stirred at that temperature overnight
  2. 2
    AutreThe organic layer was separated
  3. 3
    Lavagewashed with water and brine
  4. 4
    Séchagedried over anhydrous magnesium sulfate
  5. 5
    AutreThe solvent was evaporated under reduced pressure

Mode opératoire

Ethyl bromoacetate (0.62 mL) was added to a mixture of 5-bromo-2-hydroxyacetophenone (1.0 g) and potassium carbonate (0.96 g) in N,N-dimethylformamide (10 mL) at room temperature with stirring, and the mixture was stirred at that temperature overnight. Water and ethyl acetate were added to the reaction mixture. The organic layer was separated, washed with water and brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to afford ethyl (2-acetyl-4-bromophenoxy)acetate as a crude product.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07423185B2uspto-grants-2008_09