Reacción #11540

ord-f6144ee0e8f24ce288490dbd6a6d4c57

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturathe mixture was refluxed overnight
  2. 2
    Lavadowashed with hexane (100 ml)
  3. 3
    Otroto remove sodium hydride oil
  4. 4
    Concentraciónconcentrated under reduced pressure
  5. 5
    FiltraciónThe resulting crystals were filtered off with ethyl acetate

Procedimiento

Next, 6 N hydrochloric acid (96.8 ml, 581 mmol) was added to diethyl 2-methyl-2-(4-pyridylmethyl)malonate (17.2 g, 64.6 mmol), and the mixture was refluxed overnight. The reaction mixture was allowed to stand, then washed with hexane (100 ml) to remove sodium hydride oil contained in diethyl 2-methyl-2-(4-pyridylmethyl)malonate, and concentrated under reduced pressure. The resulting crystals were filtered off with ethyl acetate to give 10.7 g (82%) of 2-methyl-3-(4-pyridyl)propionic acid as pale pink crystals.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07098226B2uspto-grants-2006_08