Reacción #6832

ord-cf21a2c6a3124730980c313880a02012

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe solvent was evaporated
  2. 2
    Otrothe resulting residue was partitioned in 50 mL 1 N hydrochloric acid
  3. 3
    OtroThe ethyl ether phase was collected
  4. 4
    Lavadowashed with 50 mL 1 N hydrochloric acid
  5. 5
    SecadoThe ether phase was dried over sodium sulfate
  6. 6
    Otrothe solvent was evaporated

Procedimiento

A solution of 3-(4-methoxy-phenyl)acrylic acid ethyl ester (1.0 g) and tetramethyl-guanidine (125 μL) was stirred for 24 h at 70° C. in 2.5 mL nitromethane. The solvent was evaporated and the resulting residue was partitioned in 50 mL 1 N hydrochloric acid and 50 mL ethyl ether. The ethyl ether phase was collected and washed with 50 mL 1 N hydrochloric acid. The ether phase was dried over sodium sulfate and the solvent was evaporated to furnish 1.15 g of 3-(4-methoxyphenyl)-4-nitrobutyric acid ethyl ester.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07084154B2uspto-grants-2006_08