Reacción #82475

ord-45bccc0fd90f4902bf29bd9f65b6b1e9

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrofitted with a reflux condenser
  2. 2
    Temperaturathe mixture was heated
  3. 3
    Temperaturaat reflux for two days
  4. 4
    OtroThe organic materials were separated
  5. 5
    Secadodried (MgSO4)
  6. 6
    Concentraciónthen concentrated under reduced pressure
  7. 7
    OtroThe residue was purified by flash chromatography (SiO2, gradient hexane to 8:1 hexane/ethyl acetate) which

Procedimiento

Methyl 3-bromobenzoate (1.99 g, 9.25 mmol), tetrakis(triphenylphosphine) palladium(O) (110 mg), sodium carbonate (2.04 g, 19 mmol in 5 ml water) and toluene (10 ml) were degassed under nitrogen in a 25 ml flask fitted with a reflux condenser. 2-Methoxybenzeneboronic acid (1.46 g, 9.61 mmol) in toluene (1 ml) was added and the mixture was heated at reflux for two days then mixed with 1:1 saturated sodium chloride/ethyl acetate (15 ml). The organic materials were separated, dried (MgSO4) then concentrated under reduced pressure. The residue was purified by flash chromatography (SiO2, gradient hexane to 8:1 hexane/ethyl acetate) which gave methyl 3-(2-methoxyphenyl)benzoate (1.43 g, 64%), m.p.: 92°-93° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05622937uspto-grants-1997_04