Réaction #962

ord-56818a6d757b4766865fa51ce27de994

Équation de réaction

ClCC1CCN(Cc2ccccc2)C1
(3RS)-1-benzyl-3-chloromethyl pyrrolidine
[C-]#N.[Na+]
sodium cyanide
O
Water
N#CCC1CCN(Cc2ccccc2)C1
product
Rendement 92.0%
N#CCC1CCN(Cc2ccccc2)C1
(3RS)-1-benzyl-3-cyanomethyl pyrrolidine
Rendement 92.0%

Conditions de réaction

Température
60°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Extractionthe mixture was extracted three times with ethyl acetate
  2. 2
    LavageThe combined organic layer was washed with brine
  3. 3
    Séchagedried (Na2SO4)
  4. 4
    Filtrationfiltered
  5. 5
    Autreevaporated

Mode opératoire

16.8 g (0.08 mole) (3RS)-1-benzyl-3-chloromethyl pyrrolidine and 5.88 g (0.12 mole) of sodium cyanide was dissolved in 250 ml dimethyl sulfoxide. The mixture was stirred at 60° C. for two days and at room temperature for one week. Water was added and the mixture was extracted three times with ethyl acetate. The combined organic layer was washed with brine, dried (Na2SO4), filtered and evaporated to yield 14.7 g (92%) of the product.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05723444uspto-grants-1998_03