Reaktion #52857

ord-6cfff494e68e417c9ae14cf9c654253c

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Waschenby washing with 2% of hydrochloric acid, water, 95% ethanol, acetone and anhydrous ether
  2. 2
    Trocknendried in vacuum for several hours) in 6 ml of dry benzene
  3. 3
    workup.ADDITIONwas slowly added
  4. 4
    TemperaturThe resulting mixture was refluxed for 2 h
  5. 5
    FiltrationThe precipitate was filtered through celite
  6. 6
    Waschenthe filtrate was washed with cold 15% sulfuric acid
  7. 7
    WaschenThe organic phase was washed with saturated sodium bicarbonate, brine
  8. 8
    Trocknendried over Na2SO4
  9. 9
    Filtrationfiltered
  10. 10
    Einengenconcentrated
  11. 11
    Sonstigeto give a red oil
  12. 12
    SonstigePurification by flash chromatography (silica gel, 30% ethyl acetate in hexane)

Vorschrift

To a refluxing solution of zinc dust (0.15 g, 20 mesh, activated prior to use by washing with 2% of hydrochloric acid, water, 95% ethanol, acetone and anhydrous ether, then dried in vacuum for several hours) in 6 ml of dry benzene was slowly added a mixture of bromo ethyl acetate (0.082 ml, 0.74 mmol) and ethyl 4-[(5,5-dimethyl-5,6-dihydro-naphthalen-8(7H)-one-2-yl)azo]benzoate (Compound D10, 0.13 g, 0.371 mmol) in 6 ml of dry benzene. The resulting mixture was refluxed for 2 h then cooled to room temperature. The precipitate was filtered through celite and the filtrate was washed with cold 15% sulfuric acid. The organic phase was washed with saturated sodium bicarbonate, brine, dried over Na2SO4, filtered and concentrated to give a red oil. Purification by flash chromatography (silica gel, 30% ethyl acetate in hexane) afforded the title compound as a red oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06855832B2uspto-grants-2005_02