Reacción #164105

ord-a1f67065fc93401c84c485ebc986db04

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónwas extracted with ether (4×150 mL)
  2. 2
    ConcentraciónAfter the solution was concentrated
  3. 3
    Secadodried overnight with magnesium sulphate
  4. 4
    Filtraciónfiltered
  5. 5
    Otrothe solvent was removed in a vacuum

Procedimiento

40% aqueous dimethylamine solution (2.8 mL, 22.1 mmol), 4-benzyl-4-((dimethylamino)methyl)cyclohexanone (1.13 g, 4.60 mmol) and potassium cyanide (0.70 g, 11.0 mmol) were added to a mixture of 4N hydrochloric acid (3 mL) and methanol (1.05 mL) with ice cooling. The mixture was stirred for 2 d at room temperature and then after adding water (200 mL) was extracted with ether (4×150 mL). After the solution was concentrated, the residue was taken up in dichloromethane (200 mL) and dried overnight with magnesium sulphate, filtered and the solvent was removed in a vacuum. The nitrile was obtained as an oil which was crystallised through.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08835689B2uspto-grants-2014_09