Reaktion #40271

ord-c9764fada08d4935a6780c2b27f8914f

Reaktionsgleichung

[C-]#N.[K+]
potassium cyanide
CCOC(=O)CC#N
ethyl cyanoacetate
CC(C)CC=O
isovaleraldehyde
CCCCCC
hexane
[C-]#N.[K+]
potassium cyanide
CC(C)CC(C#N)CC#N
2-isobutyl-succinonitrile
Ausbeute 99.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeWhen no additional water was collected
  2. 2
    Temperaturthe mixture was cooled
  3. 3
    workup.DISTILLATIONdistilled under vacuum
  4. 4
    Sonstigeto remove solvent
  5. 5
    workup.ADDITIONIsopropanol (1 L) was added to the remaining oil
  6. 6
    workup.DISTILLATIONThe reaction mixture was distilled at atmospheric pressure until a temperature of 95° C.
  7. 7
    Temperaturrefluxed at this temperature for 5 h
  8. 8
    TemperaturThe reaction mixture was cooled
  9. 9
    workup.ADDITIONdiluted with water (0.5 L)
  10. 10
    Extraktionextracted with 1 L methyl tert-butyl ether (MTBE)
  11. 11
    ExtraktionThe MTBE extract
  12. 12
    Waschenwas washed with water (0.5 L)
  13. 13
    Trocknendried over anhydrous magnesium sulfate
  14. 14
    Filtrationfiltered
  15. 15
    Einengenconcentrated under vacuum

Vorschrift

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).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07727749B2uspto-grants-2010_06