Reacción #2460296

ord-aff65ac74f8440e3ac3a2bece001f2f0

Ecuación de reacción

O=C(O)c1ccccc1S
thiosalicylic acid
COc1ccc(I)cc1
4-iodoanisole
O=C([O-])[O-].[K+].[K+]
potassium carbonate
COc1ccc(Sc2ccccc2C(=O)O)cc1
2-(4-methoxyphenylthio)benzoic acid

Condiciones de reacción

Temperatura
165°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroby sparging with nitrogen for 10 min
  2. 2
    Temperaturacooled
  3. 3
    workup.ADDITIONThe reaction mixture was poured onto a mixture of 500 g of ice plus 40 mL or concentrated HCl
  4. 4
    OtroThe resulting precipitate was collected
  5. 5
    Lavadowashed with water
  6. 6
    Otrodried
  7. 7
    OtroThe product was purified by recrystallization from a mixture of water, ethanol, and tetrahydrofuran
  8. 8
    OtroA white powder was obtained

Procedimiento

First, 2-(4-methoxyphenylthio)benzoic acid was prepared. A stirred mixture of thiosalicylic acid (10.0 g, 65 mmol), 4-iodoanisole (15.18 g, 65 mmol), potassium carbonate (19.72 g, 143 mmol), copper powder (0.82 g, 13 mmol), and N-methylpyrrolidinone (100 mL) was deaerated by sparging with nitrogen for 10 min, heated at 165° C. for 18 h, and then cooled to ambient. The reaction mixture was poured onto a mixture of 500 g of ice plus 40 mL or concentrated HCl. The resulting precipitate was collected, washed with water, and dried. The product was purified by recrystallization from a mixture of water, ethanol, and tetrahydrofuran. A white powder was obtained, mass: 12.06 g (71% of theory).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07459263B2uspto-grants-2008_12