Reaktion #334229

ord-021c11c3d6314ad7a33c8d03d85e1b1e

Reaktionsgleichung

CC1CCCNC1
3-methylpiperidine
N#CCCCCl
4-chlorobutyronitrile
CC1CCCN(CCCC#N)C1
4-(3-methylpiperidino)-butyronitrile
Ausbeute 70.3%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe precipitate was removed by filtration
  2. 2
    SonstigeThe residue from the evaporation
  3. 3
    workup.DISTILLATIONwas purified by distillation under reduced pressure

Vorschrift

In a solution under reflux of 58.6 ml (0.50 mole) of 3-methylpiperidine in 65 ml of benzene, were run in 25 minutes 27.2 g (0.25 mole) of 4-chlorobutyronitrile Reflux was continued for 2h, the precipitate was removed by filtration and the filtrate brought to dryness under reduced pressure. The residue from the evaporation was purified by distillation under reduced pressure to give 29.2 g (yields=70.3%) of 4-(3-methylpiperidino)-butyronitrile which was in the form of a colourless oil. Boiling point 5-6 mmHg =100° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04705795uspto-grants-1987_11