Réaction #2329

ord-045379b86e3a4189977f9bacd7189198

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrethe solvent was evaporated in vacuo
  2. 2
    Autreto give an orange oil
  3. 3
    FiltrationA solution of this oil, in a small volume of dichloromethane, was filtered through silica
  4. 4
    Autrethe clear filtrate, on evaporation

Mode opératoire

Bromine (2.09 ml) was added dropwise over ten minutes to a stirred solution of the product of step (i) above (9.44 g) in carbon tetrachloride (200 ml). The solution was stirred for 16 hours, then the solvent was evaporated in vacuo to give an orange oil. A solution of this oil, in a small volume of dichloromethane, was filtered through silica and the clear filtrate, on evaporation, gave methyl 4-(2-bromo-2,2-dimethylacetyl)phenoxyacetate, 11.3 g, as a white crystalline solid: m.p. 46°-50° C.; NMR (d6DMSO) δ 8.09 (2H, d), 7.05 (2H, d), 4.92 (2H, s), 3.72 (3H, s), 2.0(6H, s).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05728701uspto-grants-1998_03