Reacción #8528

ord-ef41386ffd2e4542a863081859790979

Ecuación de reacción

[H][H]
hydrogen
O=[N+]([O-])c1ccc(F)c(F)c1F
2,3,4-Trifluoronitrobenzene
COC(=O)C(C)=O
methyl pyruvate
CCO
ethanol
O=S(=O)([O-])[O-].[Mg+2]
magnesium sulfate
CCOC(=O)C(C)Nc1ccc(F)c(F)c1F
title compound
CCOC(=O)C(C)Nc1ccc(F)c(F)c1F
Ethyl 2-(2,3,4-trifluoroanilino)propionate

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    FiltraciónAfter filtering off Pd—C and magnesium sulfate
  2. 2
    Concentraciónthe obtained filtrate was concentrated under reduced pressure
  3. 3
    OtroThe residue thus obtained

Procedimiento

2,3,4-Trifluoronitrobenzene (3.54 g) and methyl pyruvate (2.32 g) were dissolved in ethanol (30 ml). After adding 5% Pd—C (2.0 g) and anhydrous magnesium sulfate (2.65 g), the mixture was stirred at 50° C. in a hydrogen atmosphere for 16 hours. After filtering off Pd—C and magnesium sulfate, the obtained filtrate was concentrated under reduced pressure. The residue thus obtained was subjected to silica gel column chromatography (ethyl acetate-normal hexane=1:4) to give the title compound (4.84 g) as a pale yellow oily substance.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07087778B2uspto-grants-2006_08