Reaktion #4069

ord-5dcd18cf32f744b38e1a3a9e2e554156

Reaktionsgleichung

O=C1CCC(=O)N1Br
N-bromosuccinimide
COC(=O)Cc1ccccc1
methyl phenylacetate
COC(=O)C(Br)c1ccccc1
title compound
Ausbeute 93.1%
COC(=O)C(Br)c1ccccc1
Methyl Bromo-Phenylacetate
Ausbeute 93.1%

Lösungsmittel

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturto reflux
  2. 2
    Temperaturrefluxed for about 12 hours
  3. 3
    Filtrationfiltered
  4. 4
    EinengenThe filtrate was concentrated by evaporation under vacuum

Vorschrift

In this example, a mixture containing 5.93 g of N-bromosuccinimide, 5.0 g of methyl phenylacetate; and a catalytic amount (about 0.1 g) of benzoyl peroxide in 50 ml of carbon tetrachloride was warmed to reflux and then refluxed for about 12 hours. The mixture was then cooled to about 0° C. and filtered. The filtrate was concentrated by evaporation under vacuum affording 7.1 g of the title compound as an oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04723031uspto-grants-1988_02