Reaktion #1163300

ord-3f20b1c0c8744fae90252fef2d03d760

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturreflux temperature
  2. 2
    Temperaturthe mixture is maintained at its
  3. 3
    Temperaturreflux temperature for an additional hour
  4. 4
    FiltrationThe reaction mixture is filtered while hot, the residue
  5. 5
    Waschenwashed with boiling chloroform
  6. 6
    Sonstigethe combined filtrates evaporated to dryness in vacuo
  7. 7
    workup.DISSOLUTIONThe residue is dissolved in a minimum of methylene chloride
  8. 8
    Wascheneluted with methylene chloride
  9. 9
    EinengenThe eluate is concentrated

Vorschrift

Commercially available 4-methyl-1-tetralone, 32.0 grams, contained in 250 ml. of chloroform and 50 ml. of ethyl acetate is heated to boiling. A mixture of 98.3 grams of cupric bromide and 50 ml. of ethyl acetate is heated to its reflux temperature. After all of the hydrogen bromide is evolved, the mixture is maintained at its reflux temperature for an additional hour. The reaction mixture is filtered while hot, the residue washed with boiling chloroform and the combined filtrates evaporated to dryness in vacuo. The residue is dissolved in a minimum of methylene chloride, placed upon an alumina column and eluted with methylene chloride. The eluate is concentrated and the desired 2-bromo-4-methyl-1-tetralone obtained as a dark oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US03954983uspto-grants-1976_05