Reacción #318838
ord-d7ef2083fe1c4c5099d4d95006f7031d
Ecuación de reacción
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1Temperaturathe mixture is refluxed
- 2Otrothe toluenic portion is separated
- 3Extracciónthe aqueous phase is extracted with toluene
- 4Lavadowashed with water and saturated brine (aqueous sodium chloride solution) until the reaction
- 5Secadoit is dried over anhydrous sodium sulfate
- 6OtroFinally, the solvent is evaporated under reduced pressure
- 7workup.DISTILLATIONthe residue is distilled
Procedimiento
To a boiling solution of 2-(2-methylphenyl)-3-methylbutyronitrile (Herz W., J.Am.Chem.Soc. 80, 3139, 1958) (207.9 g) and 86% 3,3-diethoxypropylchloride (154 g) in anhydrous toluene (1250 ml) is dropped during about 50 minutes under stirring 107.7 g of a 50% toluenic sodium amide suspension (NaNH2 content 53.8 g) and the mixture is refluxed under continuous stirring for 6 hours. On subsequent cooling, the stirred mixture is diluted with water (300 ml), the toluenic portion is separated and the aqueous phase is extracted with toluene. The organic solutions are combined, washed with water and saturated brine (aqueous sodium chloride solution) until the reaction is neutral, and then it is dried over anhydrous sodium sulfate. Finally, the solvent is evaporated under reduced pressure and the residue is distilled to give 302.9 g (83.2%) of 5,5-diethoxy-2-isopropyl-2-(2-methylphenyl-valeronitrile, b.p. 102° to 104° C. at 4 Pa.