Reacción #46725

ord-4ee9517eb9ec420cb4980422cdb446dd

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónextracted with diethylether (30 mL)
  2. 2
    SecadoThe organic phase was dried (MgSO4)
  3. 3
    Filtraciónfiltered
  4. 4
    Otrothe eluate evaporated

Procedimiento

To a solution of N-(2,4-dihydroxy phenyl)-2,2,2-trifluoro-acetamide (0.44 g; 2 mmol) in DMF (4 mL) was added K2CO3 and 1-bromooctane (0.37 mL; 2.1 mmol). The slurry was stirred for 2 days at room temperature, poured onto 0.1 M HCl (aq.; 50 mL) and then extracted with diethylether (30 mL). The organic phase was dried (MgSO4), filtered and the eluate evaporated to leave 550 mg of black solid which was purified by chromatography (SiO2; PE80-100° C./EtOAc=4:1) to leave 100 mg (15%) of a pure white solid. Mp. 114-116° C.; MS (GC-MS; Cl): 334 (MH+).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07741352B2uspto-grants-2010_06