Reacción #3013
ord-7722dbce85914723bdf979fd6d719ccd
Ecuación de reacción
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Temperaturathe reaction mixture is heated
- 2Temperaturaat reflux for 18 hours
- 3Otrois removed as it
- 4Otrois formed in the reaction mixture
- 5OtroThe toluene is evaporated
Procedimiento
4.2 g of 2,6-dimethoxy-4-methylaniline are dissolved in 50 ml of toluene, 2.45 g of cyclohexanone are then added and the reaction mixture is heated at reflux for 18 hours. The water which is formed is removed as it is formed in the reaction mixture using a Dean and Stark apparatus. The toluene is evaporated and the oily N-cyclohexylidene-2,6-dimethoxy-4-methylaniline residue obtained is used without addition of purification in the following stage.