Reacción #157911

ord-c6d317735b2344efb16480c76fdf15f4

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroprecipitation after a few minutes
  2. 2
    ConcentraciónThe reaction mixture was concentrated in vacuo
  3. 3
    Otropurified by flash chromatography (eluent: EtOAc (0-10%) in heptane)
  4. 4
    Otroaffording 517 mg (1.14 mmol; 93%) of colourless oil

Procedimiento

To a stirred solution at room temperature of 4-(1-phenylcyclohexyl)phenol (311 mg, 1.23 mmol) in dry THF (2 mL) was added BocValOH (295 mg, 1.36 mmol) dissolved in THF (2 mL). A solution of DIC (231 μL; 1.48 mmol) in THF (2 mL) was added drop wise, which caused precipitation after a few minutes. After 5 min DMAP (166 mg; 1.36 mmol) was added and stirring was continued for 19 h. The reaction mixture was concentrated in vacuo and purified by flash chromatography (eluent: EtOAc (0-10%) in heptane) affording 517 mg (1.14 mmol; 93%) of colourless oil. LC-MS purity (UV/MS): 100/100%, Rt 6.77 min, M+18: 469.53.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08822548B2uspto-grants-2014_09