Reacción #93742

ord-eb0b16f76c204a91b8b24382161ff25e

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    LavadoThe solution is washed with saturated aqueous NH4Cl and water
  2. 2
    Otrodried
  3. 3
    Otroevaporated in vacuo
  4. 4
    Otroto give an oil
  5. 5
    OtroPurification on a silica gel
  6. 6
    Otrodry column

Procedimiento

To a solution of 1.85 g (5 mmol) of 2,5,9-trimethyl-11-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8,10-undecapentaenyl acetate in 25 ml of anhydrous THF and 8 ml of HMPA is added in portions 0.68 g (5.2 mmol) of sodium thiophenoxide. The resulting mixture is stirred at room temperature for 18 hours and then taken up in 250 ml of diethyl ether. The solution is washed with saturated aqueous NH4Cl and water, dried and evaporated in vacuo to give an oil. Purification on a silica gel dry column gives the desired product.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04614747uspto-grants-1986_09