Reacción #50360

ord-886f87c09f3e4a15999176d8eab283ce

Disolventes

Condiciones de reacción

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

Tratamiento posterior

  1. 1
    Otroat 0° C.
  2. 2
    OtroThe layers were separated
  3. 3
    Extracciónextracted with ether (3×5 ml)
  4. 4
    Lavadowashed with 5% NaHCO3 (2×1 ml), brine (1×1 ml)
  5. 5
    Secadodried over MgSO4
  6. 6
    Concentraciónconcentrated

Procedimiento

(2R,3S,4S,5R)-5-(Triethylsilyloxy)-2,3-epoxy-2,4-dimethyl-1-octanol (21.0 mg, 69.4 μmol) in 300 μl of THF at 0° C. was deprotonated with 1.05 eq of n-butyllithium. After 15 min, 0.1M samarium diiodide (764 μmol, 1.1 eq) was added and the reaction was allowed to warm to 25° C. over night. Then 1 ml of 1/2 saturated Rochelle's salt was added, stirred an additional 1 h, and poured onto 5 ml of Et2O and 1 ml of H2O. The layers were separated, extracted with ether (3×5 ml), washed with 5% NaHCO3 (2×1 ml), brine (1×1 ml), dried over MgSO4 and concentrated to give 31 crude.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05426206uspto-grants-1995_06