反应 #792143
ord-9093db35302043bdb647894439ed066a
反应方程式
(E)-1-(2-hydroxy-4,5-dimethylphenyl)-3-(pyridine-2-yl)prop-2-en-1-one
→
final compound
收率 49.2%
1-(2-hydroxy-4,5-dimethylphenyl)-3-(pyridine-2-yl)propan-1-one
收率 49.2%
溶剂
反应条件
详细条件
See reaction.notes.procedure_details.
后处理
- 1过滤the catalyst was filtered off
- 2其他The crude product was purified by chromatography on silica gel (20% EtOAc/hexane)
实验过程
In a 250 ml round-bottom flask, (E)-1-(2-hydroxy-4,5-dimethylphenyl)-3-(pyridine-2-yl)prop-2-en-1-one (1.17 g, 4.62 mmol) and 0.18 g of 10% Pd/C were mixed together in wet EtOAc. Hydrogenation was conducted at atmospheric pressure, then the catalyst was filtered off. The crude product was purified by chromatography on silica gel (20% EtOAc/hexane) to provide 0.58 g (47.7%) of final compound.