Reacción #5399

ord-5e5c25f893b444bd9bf8ae43f97a4d3f

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Lavadowashed once with sodium carbonate solution and twice with water
  2. 2
    Secadosubsequently dried over magnesium sulfate
  3. 3
    Filtraciónfiltered
  4. 4
    Concentraciónconcentrated
  5. 5
    OtroThe crude product was purified by chromatography on silica gel with toluene/ethyl acetate (vol. 9:1)
  6. 6
    OtroRecrystallization from ethyl acetate at -20° C.

Procedimiento

A solution of 3.0 g of trans-4-(4'-cyano-4-biphenylyl)cyclohexanol, 1.1 ml of 3,4-dihydro-2H-pyran in 30 ml of dichloromethane was treated at 0° C. with a solution of 0.007 g of bistrimethylsilyl sulfate in 2 ml of dichloromethane. The reaction mixture was stirred at 0° C. for a further 30 minutes and then washed once with sodium carbonate solution and twice with water and subsequently dried over magnesium sulfate, filtered and concentrated. The crude product was purified by chromatography on silica gel with toluene/ethyl acetate (vol. 9:1). Recrystallization from ethyl acetate at -20° C. gave 1.75 g of pure trans-4-(4'-cyano-4-biphenylyl)cyclohexyl tetrahydropyranyl ether.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05244597uspto-grants-1993_09