Reacción #214428

ord-ab0364e7a0db4563a625514310be0b19

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    FiltraciónThe catalyst was filtered off
  2. 2
    Otrothe filtrate evaporated under reduced pressure to a solid, which
  3. 3
    Otrowas triturated under acetone
  4. 4
    Filtraciónfiltered
  5. 5
    Otroto give a total yield of product of 2.9 g (43%), mp 230° C. (dec)

Procedimiento

1-Benzyl-4-(2-hydroxy-3-n-hexadecyloxypropyl)-piperazine hydrochloride (8 g, 0.0146 mol) was dissolved in toluene (100 ml), methanol (100 ml) and tetrahydrofuran (700 ml) and divided into three 300 ml portions. Each portion was hydrogenated overnight at room temperature on a Parr shaker using a 10% palladium on carbon catalyst (2 g) and 50 p.s.i.g. hydrogen. The catalyst was filtered off and the filtrate evaporated under reduced pressure to a solid, which was triturated under acetone and filtered to give a total yield of product of 2.9 g (43%), mp 230° C. (dec).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04255426uspto-grants-1981_03