Reacción #44170

ord-43c5c0c66d5a4557aba3851a4a0e8ac7

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturacooled to 0 C
  2. 2
    workup.STIRRINGstirred for a further 3 h
  3. 3
    Extracciónextracted with ethyl acetate
  4. 4
    LavadoThe combined organic phases were washed with brine
  5. 5
    Secadodried (sodium sulfate)
  6. 6
    Concentraciónconcentrated
  7. 7
    OtroThe crude was purified by column chromatography (SPE cartridge, SiO2)

Procedimiento

A solution of borane (1M, THF, 2.5 eq., 38.2 mL) was added dropwise to a stirred solution of (3-iodophenyl)acetic acid (4.0 g) in THF (100 mL) cooled to 0 C. The resulting mixture was stirred at 0 C for 1 h then warmed to room temperature and stirred for a further 3 h. The mixture was poured into aqueous ammonium chloride solution and extracted with ethyl acetate. The combined organic phases were washed with brine, dried (sodium sulfate) and concentrated. The crude was purified by column chromatography (SPE cartridge, SiO2), using cyclohexane-ethyl acetate (70:30) as eluent to afford the title compound (3.5 g, 92% yield).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07732600B2uspto-grants-2010_06