Reaktion #9720

ord-5d337718b4324e0dae33ac3f4b6f3bab

Reaktionsgleichung

CC(=O)c1ccc(O)c(C)c1
1-(4-Hydroxy-3-methylphenyl)ethanone
O=C([O-])[O-].[Cs+].[Cs+]
cesium carbonate
CCOC(=O)CBr
ethyl bromoacetate
O=C([O-])[O-].[Cs+].[Cs+]
cesium carbonate
CCOC(=O)CBr
Ethyl bromoacetate
CCOC(=O)COc1ccc(C(C)=O)cc1C
title compound
CCOC(=O)COc1ccc(C(C)=O)cc1C
ethyl(4-acetyl-2-methylphenoxy)acetate

Lösungsmittel

Reaktionsbedingungen

Temperatur
40°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturheating
  2. 2
    workup.WAITcontinued for a further hour
  3. 3
    SonstigeThe cooled reaction
  4. 4
    Filtrationwas filtered
  5. 5
    Einengenthe filtrate concentrated

Vorschrift

1-(4-Hydroxy-3-methylphenyl)ethanone (90 g) and cesium carbonate (216 g) were stirred in acetonitrile (900 ml) at room temperature under nitrogen for 10 minutes. Ethyl bromoacetate (73 ml) was added and the mixture heated to 40° C. for 3 hours. Further ethyl bromoacetate (2.5 ml) and cesium carbonate (1 g) were added and heating continued for a further hour. The cooled reaction was filtered and the filtrate concentrated to give the title compound as a yellow oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07091237B2uspto-grants-2006_08