Reacción #64908

ord-46a158f26c644bbb9e76a987e6d0e912

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaat reflux for 1 h
  2. 2
    Temperaturato cool
  3. 3
    LavadoThe organic solution was washed with saturated aqueous sodium carbonate solution (3×15 mL) and water (3×15 mL)
  4. 4
    Secadodried over magnesium sulfate
  5. 5
    Concentraciónconcentrated under reduced pressure
  6. 6
    OtroThe reaction product was purified by flash chromatography

Procedimiento

A solution of 7-hydroxy-7-methyl-7,8,9,10-tetrahydroacephenanthrene (0.15 g, 0.64 mmol) and camphorsulfonic acid (0.02 g, 0.064 mmol) in toluene (20 mL) was heated at reflux for 1 h. The reaction was allowed to cool and was diluted with ethyl acetate (20 mL). The organic solution was washed with saturated aqueous sodium carbonate solution (3×15 mL) and water (3×15 mL), dried over magnesium sulfate, and concentrated under reduced pressure. The reaction product was purified by flash chromatography to give 0.13 g (92%) of the product: MS (CI) m/e (%) 221 (M+H+, 100); 1H NMR (CDCl3, 300 MHz) δ 7.69 (d, 1H, J=8.4 Hz), 7.44 (dd, 1H, J=7.0, 8.4 Hz), 7.32 (s, 1H), 7.21 (d, 1H, J=6.9 Hz), 5.94 (m, 1H), 3.38 (s, 4H), 3.09 (t, 2H, J=8.5 Hz), 2.52 (m, 2H), 2.16 (m, 3H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05416089uspto-grants-1995_05