Reacción #1340622

ord-1eb518f4a2944255b708f35cfd0d8c29

Ecuación de reacción

Cl.Cl.NCc1ccccc1
benzylamine dihydrochloride
CCN(C(C)C)C(C)C
diisopropylethylamine
COC(=O)CC(=O)CC(=O)OC
dimethyl 3-oxopentanedioate
COC(=O)Cc1cc(O)n(Cc2ccccc2)n1
methyl (1-benzyl-5-hydroxy-1H-pyrazol-3-yl)acetate
Rendimiento 64.2%

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: US08455486B2uspto-grants-2013_06