Reacción #1255

ord-b9c7d389a33241bbb79d7412a80e13bc

Ecuación de reacción

CCCCCCCCCCOc1cnc(-c2ccc(C=CCCO)cc2)nc1
2-(4-(4-hydroxy-1-butenyl) phenyl)-5-decyloxypyrimidine
[H][H]
hydrogen
[H][H]
hydrogen
CCCCCCCCCCOc1cnc(-c2ccc(CCCCO)cc2)nc1
2-(4-(4-hydroxybutyl)-phenyl)-5-decyloxypyrimidine
Rendimiento 99.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrowas consumed
  2. 2
    FiltraciónThen 10% Pd/C was filtered out
  3. 3
    Concentraciónthe filtrate was concentrated

Procedimiento

0.38 g (1 mmol) of the thus obtained 2-(4-(4-hydroxy-1-butenyl) phenyl)-5-decyloxypyrimidine was dissolved in 20 ml of tetrahydrofuran, added with 0.05 g of 10% Pd/C and subjected to a hydrogenation reaction in a hydrogen atmosphere under normal pressure. The reaction was stopped when about 25 ml of hydrogen was consumed. Then 10% Pd/C was filtered out and the filtrate was concentrated to obtain 0.38 g of 2-(4-(4-hydroxybutyl)-phenyl)-5-decyloxypyrimidine (yield: 99%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05723610uspto-grants-1998_03