Reacción #1797520

ord-779eb53f8c4a4c94b31b981fb1fb4b7d

Condiciones de reacción

Temperatura
70°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otro(reaction progress monitored by TLC)
  2. 2
    Lavadowashed with dichloromethane (3×200 mL)
  3. 3
    SecadoThe organic layer was dried over magnesium sulfate
  4. 4
    Otroevaporated

Procedimiento

To a solution of 5-chloro-1-phenyl-1H-pyrazole-4-carboxylic acid ethyl ester (Intermediate 1; 7.3 g, 29.1 mmol) in tetrahydrofuran (70 mL) was added a solution of lithium hydroxide in water (7.3 g, 305 mmol) in water (70 mL). Methanol (˜10 mL) was added dropwise to the reaction mixture until only one layer was visible. The reaction mixture was stirred at 70° C. for 1 hour (reaction progress monitored by TLC). The reaction mixture was acidified to pH 3 with 1N hydrochloric acid and washed with dichloromethane (3×200 mL). The organic layer was dried over magnesium sulfate and evaporated to give 5-chloro-1-phenyl-1H-pyrazole-4-carboxylic acid (5.8 g, 91%), which HPLC analysis indicated was 85% pure. This material was used directly in the next step without further purification.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07790711B2uspto-grants-2010_09