Reacción #46196

ord-b6070459a8bd4343bdcbabd12aa6e6b6

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturawas cooled to 0° C
  2. 2
    Filtraciónfiltered
  3. 3
    ExtracciónThe filtrate was extracted with EtOAc (500 mL×3)
  4. 4
    SecadoThe combined organic layers were dried over anhydrous Na2SO4
  5. 5
    Otroevaporated under reduced pressure

Procedimiento

To a solution of 3,4,5-trihydroxy-benzoic acid methyl ester (50 g, 0.27 mol) and Na2B4O7 (50 g) in water (1000 mL) was added Me2SO4 (120 mL) and aqueous NaOH solution (25%, 200 mL) successively at room temperature. The mixture was stirred at room temperature for 6 h before it was cooled to 0° C. The mixture was acidified to pH ˜2 by adding conc. H2SO4 and then filtered. The filtrate was extracted with EtOAc (500 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and evaporated under reduced pressure to give methyl 3,4-dihydroxy-5-methoxybenzoate (15.3 g 47%), which was used in the next step without further purification.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07741321B2uspto-grants-2010_06