反应 #1255

反应方程式

2-(4-(4-hydroxy-1-butenyl) phenyl)-5-decyloxypyrimidine

hydrogen

hydrogen

→

2-(4-(4-hydroxybutyl)-phenyl)-5-decyloxypyrimidine

收率 99.0%

溶剂

tetrahydrofuran

反应条件

后处理

1. 1
   其他was consumed
2. 2
   过滤Then 10% Pd/C was filtered out
3. 3
   浓缩the filtrate was concentrated

实验过程

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%).

来源