Reacción #347517

ord-06486d071e464a83afeca12d65d77088

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroat room temperature
  2. 2
    Otroovernight
  3. 3
    ExtracciónThe reaction was extracted one time with 1N HCl, multiple times with saturated Na2CO3
  4. 4
    Secadodried (MgSO4)
  5. 5
    Otrothe solvent removed under reduced pressure

Procedimiento

A solution of the carbonate prepared in Example 1 (10.0 g, 28.4 mmol) in 75 mL of methylene chloride was added under nitrogen dropwise to a solution of 6-amino-1-hexanol (3.34 g, 28.4 mmol) and triethylamine (19.8 mL, 142 mmol) in 100 mL of methylene chloride at ice-bath temperature. The reaction was stirred at ice bath temperature for approximately eight hours and at room temperature overnight. The reaction was extracted one time with 1N HCl, multiple times with saturated Na2CO3, dried (MgSO4) and the solvent removed under reduced pressure to give 8.1 g of a solid. Recrystallization of the solid from diisopropyl ether gave 6.55 g (70%) of the title compound as a white crystalline solid, mp 72°-75° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05527804uspto-grants-1996_06