Reacción #2517

ord-c4ba4a81e15b4995a5093c01878efc4c

Ecuación de reacción

O=C([O-])O.[Na+]
sodium bicarbonate
COc1ccccc1N
o-anisidine
O=C(O)c1ccc([N+](=O)[O-])cc1
4-nitrobenzoic acid
CCN=C=NCCCN(C)C.Cl
1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride
COc1ccccc1NC(=O)c1ccc([N+](=O)[O-])cc1
title compound
Rendimiento 87.5%
COc1ccccc1NC(=O)c1ccc([N+](=O)[O-])cc1
4-Nitro-N-(2-methoxyphenyl)benzamide
Rendimiento 87.5%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaWith cooling in an ice bath
  2. 2
    Extracciónextracted with methylene chloride
  3. 3
    Lavadowashed with water and saturated brine in that order
  4. 4
    SecadoAfter drying on anhydrous magnesium sulfate
  5. 5
    Otrothe solvent was removed by evaporation
  6. 6
    Otrothe resulting solid material was purified by silica gel column chromatography (methylene chloride)

Procedimiento

With cooling in an ice bath, 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC.HCl) (630 mg, 3.29 mmol) was added to 15 ml of methylene chloride solution containing o-anisidine (368 mg, 2.99 mmol) and 4-nitrobenzoic acid (500 mg, 2.99 mmol). After 1 hour of stirring at the same temperature, the reaction mixture was roughly adjusted to pH 8 with saturated sodium bicarbonate aqueous solution, extracted with methylene chloride and then washed with water and saturated brine in that order. After drying on anhydrous magnesium sulfate, the solvent was removed by evaporation, and the resulting solid material was purified by silica gel column chromatography (methylene chloride) to obtain 712 mg (87.4%) of the title compound in the form of yellow powder.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05728835uspto-grants-1998_03