Reacción #75948

ord-915b532ef5aa4c6983c86cbc722a0c1a

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ExtracciónThe solution was then extracted three times with ethyl acetate
  2. 2
    Lavadothe organic phase was washed sequentially with sodium hydroxide, water and brine
  3. 3
    Secadodried over sodium sulfate
  4. 4
    Concentraciónconcentrated in vacuo
  5. 5
    Otroto provide the product which
  6. 6
    Otrowas used without further purification

Procedimiento

To a solution of 4-(2-methoxyethyl)phenol (42 mg, 0.275 mmol) and (2S)-(+)-glycidyl tosylate (57 mg, 0.25 mmol) in 2 mL of DMF was added 15 mg (0.625 mmol) of sodium hydride (60% in mineral oil). The resulting mixture was allowed to stir for 16 hours at room temperature. The solution was then extracted three times with ethyl acetate, and the organic phase was washed sequentially with sodium hydroxide, water and brine, dried over sodium sulfate, and concentrated in vacuo to provide the product which was used without further purification. m/z 208 [M+H]+.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06699860B2uspto-grants-2004_03