Reacción #40271
ord-c9764fada08d4935a6780c2b27f8914f
Ecuación de reacción
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1OtroWhen no additional water was collected
- 2Temperaturathe mixture was cooled
- 3workup.DISTILLATIONdistilled under vacuum
- 4Otroto remove solvent
- 5workup.ADDITIONIsopropanol (1 L) was added to the remaining oil
- 6workup.DISTILLATIONThe reaction mixture was distilled at atmospheric pressure until a temperature of 95° C.
- 7Temperaturarefluxed at this temperature for 5 h
- 8TemperaturaThe reaction mixture was cooled
- 9workup.ADDITIONdiluted with water (0.5 L)
- 10Extracciónextracted with 1 L methyl tert-butyl ether (MTBE)
- 11ExtracciónThe MTBE extract
- 12Lavadowas washed with water (0.5 L)
- 13Secadodried over anhydrous magnesium sulfate
- 14Filtraciónfiltered
- 15Concentraciónconcentrated under vacuum
Procedimiento
A mixture of ethyl cyanoacetate (73.3 g, 6.48 mol), isovaleraldehyde (613.9 g, 7.13 mol), piperidine (5.5 g, 0.065 mol), and hexane (0.5 L) was placed under reflux with continuous removal of water. When no additional water was collected, the mixture was cooled and distilled under vacuum to remove solvent. Isopropanol (1 L) was added to the remaining oil, followed by a solution of potassium cyanide (422 g, 6.48 mol) in water (2 L). The reaction mixture was maintained below 35° C. during addition of the potassium cyanide solution and then held at approximately 35° C. for 4 h. The reaction mixture was distilled at atmospheric pressure until a temperature of 95° C. was reached and then refluxed at this temperature for 5 h. The reaction mixture was cooled, diluted with water (0.5 L) and extracted with 1 L methyl tert-butyl ether (MTBE). The MTBE extract was washed with water (0.5 L), dried over anhydrous magnesium sulfate, filtered, and concentrated under vacuum to give 873.4 g of 2-isobutyl-succinonitrile as an oil. Purified samples of 2-isobutyl-succinonitrile can be obtained by vacuum distillation (90° C. at 0.275 mm Hg).