Reacción #6607

ord-29b56e7bfb744771ab87ed2781bf6d17

Disolventes

Condiciones de reacción

Temperatura
25°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrothe phases were separated
  2. 2
    ExtracciónThe aqueous phase was extracted with ether
  3. 3
    Extracciónthe organic extract
  4. 4
    Lavadowas washed with saturated tartaric acid solution and water
  5. 5
    Secadodried over Na2SO4
  6. 6
    Concentraciónconcentrated
  7. 7
    OtroRecrystallization from reethanol

Procedimiento

15.5 ml (19.7 mmol) of diisobutylaluminum hydride solution (20% in hexane) were added dropwise under nitrogen to a solution of 3 g (9.4 mmol) of 4-cyanobenzyl 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl ether in 40 ml of dry ether at 25° C. The mixture was stirred at 25° C. for 40 min and then 250 ml of saturated tartaric acid solution were added dropwise. Subsequently, a little sodium sulfate solution was added, and the phases were separated. The aqueous phase was extracted with ether, and the organic extract was washed with saturated tartaric acid solution and water, dried over Na2SO4 and concentrated. Recrystallization from reethanol resulted in 1.4 g of the title compound of melting point 102°-104° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05248823uspto-grants-1993_09