Reaktion #2347173

ord-50ff0cd1113b4ed795f636d0807702da

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigewas recooled to 0° C.
  2. 2
    Extraktiontaken-up in water and extracted three times with methylene chloride
  3. 3
    WaschenThe organic layers were washed with 1N HCl, water, brine
  4. 4
    Trocknendried (MgSO4)
  5. 5
    SonstigeSolvent was removed in-vacuo
  6. 6
    Sonstigethe resulting residue purified

Vorschrift

To a suspension of 6.71 g (50.3 mmol) of aluminum chloride in methylene chloride at 0° C. under argon was added a solution of 3.95 g (3.58 mL, 50.3 mmol) of acetyl chloride and 10.21 g (41.9 mmol) of 5,6,7,8-tetrahydro-3,5,5,8,8-pentamethylnaphthalene in methylene chloride. The resulting mixture was allowed to warm to room temperature over a period of 3 hours with stirring. The mixture was recooled to 0° C. and 1N HCl was dropwise added. The mixture was then taken-up in water and extracted three times with methylene chloride. The organic layers were washed with 1N HCl, water, brine, and dried (MgSO4). Solvent was removed in-vacuo and the resulting residue purified using flash chromatography to give the title compound as an ivory solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05475113uspto-grants-1995_12