Reacción #1555983

ord-2de80d539bdb4387ac4215c0d054c2cf

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe resulting mixture was heated
  2. 2
    Temperaturaat reflux for 18 h
  3. 3
    Concentraciónbefore being concentrated in vacuo
  4. 4
    OtroThe resulting brown oil was purified by flash chromatography over SiO2 (CH2Cl2:MeOH, 97:3)

Procedimiento

To a suspension of benzylamine dihydrochloride (1.000 g, 5.126 mmol, 1 equiv.) in anhydrous toluene (25 ml) were added successively diisopropylethylamine (1.32 ml, 10.252 mmol, 2 equiv) and dimethyl 3-oxopentanedioate (0.893 g, 5.126 mmol, 1 equiv.). The resulting mixture was heated at reflux for 18 h before being concentrated in vacuo. The resulting brown oil was purified by flash chromatography over SiO2 (CH2Cl2:MeOH, 97:3). 0.810 g of pure methyl(1-benzyl-5-hydroxy-1H-pyrazol-3-yl)acetate was obtained as a white solid. Yield 64%. MS (ESI+): 247.1; MS (ESI−): 245.1.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09006238B2uspto-grants-2015_04