Reaktion #669384

ord-5ecfdcfbe9494c28b0be488c71647880

Reaktionsgleichung

COc1ccc(CCC(=O)O)cc1
3-(4-methoxyphenyl)propionic acid
BrBr
bromine
COc1ccc(CCC(=O)O)cc1Br
title compound
Ausbeute 87.0%
COc1ccc(CCC(=O)O)cc1Br
3-(3-Bromo-4-methoxyphenyl)propionic acid
Ausbeute 87.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionextracted with ethyl acetate
  2. 2
    WaschenThe extract was washed serially with saturated saline and water
  3. 3
    Trocknendried over anhydrous magnesium sulfate
  4. 4
    workup.DISTILLATIONthe solvent was distilled off under reduced pressure
  5. 5
    WaschenThe residue was washed with hexane

Vorschrift

To a solution of 3-(4-methoxyphenyl)propionic acid (4.0 g, 22.2 mmol) in acetic acid (20 ml) was added bromine (3.9 g, 24.4 mmol) gradually dropwise at 10° C. and the mixture was stirred at room temperature for 30 minutes. This reaction mixture was diluted with water and extracted with ethyl acetate. The extract was washed serially with saturated saline and water and dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was washed with hexane to provide the title compound (yield 5.0 g, 87%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05922771uspto-grants-1999_07