Réaction #2254223

ord-22e1fb1b43d44eb196b63e7ece641882

Solvants

Conditions de réaction

Température
120°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.ADDITIONthe resulting mix
  2. 2
    workup.ADDITIONthe reaction mix
  3. 3
    Températurewas cooled
  4. 4
    Extractionthe product was extracted by Et2O (3×400 ml)
  5. 5
    Lavagewashed with water (200 ml)
  6. 6
    Séchagedried (Na2SO4)
  7. 7
    Concentrationconcentrated
  8. 8
    Autrethe residual was purified by flash chromatography (340 g silica gel column
  9. 9
    Lavageeluted by EtOAc in hexane

Mode opératoire

Ethylene glycol (300 ml) was added to methyl 2-cyano-2-[9-(pyridin-2-yl)-6-oxaspiro[4.5]decan-9-yl]acetate (15.43 g, 49 mmol) followed by potassium hydroxide (5.5 g, 98 mmol), the resulting mix was heated to 120° C., after 3 h, the reaction mix was cooled and water (300 ml) was added, the product was extracted by Et2O (3×400 ml), washed with water (200 ml), dried (Na2SO4) and concentrated, the residual was purified by flash chromatography (340 g silica gel column, eluted by EtOAc in hexane: 3% 2 CV; 3-25%, 12 CV; 25-40% 6 CV to give 2-[9-(Pyridin-2-yl)-6-oxaspiro[4.5]decan-9-yl]acetonitrile (10.37 g, 82% yield, m/z 257.0 [M+H]+ observed).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09044469B2uspto-grants-2015_06