Reacción #57696

ord-0caaa670807f47549ceaacc50ff704c3

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    LavadoThe reaction mixture was washed with brine
  2. 2
    Extracciónextracted with ethyl acetate
  3. 3
    LavadoThe combined ethyl acetate layers were washed with brine
  4. 4
    OtroRemoval of the solvent

Procedimiento

To 748 mg (2 mmol) of 5-iodo-4-hydroxy-3-methyl-benzofuran-2-carboxylic acid tert-butyl ester was added 1.42 g (10 mmol) of iodomethane, 553 mg (4 mmol) of K2CO3 and 10 mL of DMF. The mixture was stirred at room temperature overnight. The reaction mixture was washed with brine and extracted with ethyl acetate. The combined ethyl acetate layers were washed with brine. Removal of the solvent gave 790 mg (100% yield) of 5-iodo-4-methoxy-3-methyl-benzofuran-2-carboxylic acid tert-butyl ester as a pale brown oil.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07420001B2uspto-grants-2008_09