Reacción #657257

ord-852f47be86574ff68e08c58c5bd293f0

Ecuación de reacción

CCOCc1cnn(C(c2ccccc2)(c2ccccc2)c2ccccc2)c1
1-trityl-4-ethoxymethylpyrazole
CCOCc1cn[nH]c1
4-ethoxymethylpyrazole
Rendimiento 44.0%

Reactivos

Ninguno

Condiciones de reacción

Temperatura
80°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONwas added to the resulting solution
  2. 2
    TemperaturaAfter cooling to room temperature
  3. 3
    Filtraciónthe reaction mixture was filtered
  4. 4
    Lavadowashed with dichloromethane
  5. 5
    Extracciónextracted with dichloromethane
  6. 6
    Secadodried over MgSO4
  7. 7
    Otrothe solvent was evaporated under vacuum

Procedimiento

1-trityl-4-ethoxymethylpyrazole (1.800 g, 4.88 mmol) was dissolved in a mixture of ethanol/acetone (15 ml/5 ml) and 30 mL of 2N HCl was added to the resulting solution. The mixture was heated at 80° C. for 2 h. After cooling to room temperature, the reaction mixture was filtered and washed with dichloromethane. The aqueous layer was basified with 2N NaOH and extracted with dichloromethane. The organic layers were combined, dried over MgSO4 and the solvent was evaporated under vacuum yielding compound 4-ethoxymethylpyrazole as a white oil. Yield: 44% (270 mg, 2.14 mmol).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09023315B2uspto-grants-2015_05