Reacción #363176

ord-e1d948e4bff14b87b806b0d181e33941

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturacooling
  2. 2
    LavadoThe reaction mixture was washed with 1N hydrochloric acid
  3. 3
    Secadoa saturated aqueous sodium bicarbonate solution subsequently, and dried over anhydrous magnesium sulfate
  4. 4
    OtroRemoval of the solvent in vacuo

Procedimiento

To a stirred solution of 2,5-dimethylaniline (5.30 g) and 4-dimethylaminopyridine (6.41 g) in dichloromethane (90 ml) was added acetic anhydride (4.13 ml) under ice-cooling, and the mixture was stirred for 4 hours. The reaction mixture was washed with 1N hydrochloric acid and a saturated aqueous sodium bicarbonate solution subsequently, and dried over anhydrous magnesium sulfate. Removal of the solvent in vacuo gave 2′,5′-dimethylacetanilide (6.09 g).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06353025B1uspto-grants-2002_03