Reacción #8529

ord-c97f457d75724fd29a32be088e5f8a4c

Ecuación de reacción

[H][H]
hydrogen
Nc1ccc(F)c(F)c1F
2,3, 4-Trifluoroaniline
CCOC(=O)C(C)=O
ethyl pyruvate
O=S(=O)([O-])[O-].[Mg+2]
magnesium sulfate
CCOC(=O)C(C)Nc1ccc(F)c(F)c1F
title compound
Rendimiento 95.0%
CCOC(=O)C(C)Nc1ccc(F)c(F)c1F
Ethyl 2-(2,3,4-trifluoroanilino)propionate
Rendimiento 95.0%

Disolventes

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

Procedimiento

2,3, 4-Trifluoroaniline (2.94 g) and ethyl pyruvate (2.32 g) were dissolved in methanol (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 obtained residue was subjected to silica gel column chromatography (ethyl acetate-normal hexane=1:4) to thereby give the title compound (4.69 g) as a pale yellow oily substance. Various spectral data of this product was identical with those obtained in Example 7.

Fuente

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