反应 #2298644
ord-f5e608738e7d4609bb79674cc2701688
反应方程式
4-[2-[2-ethyl-4-methyl-6-oxo-1,6-dihydro-1-pyrimidinyl]ethoxy]nitrobenzene
hydrogen
→
title compound
收率 70.0%
4-[2-[2-Ethyl-4-methyl-6-oxo-1,6-dihydro-1-pyrimidinyl]ethoxy]aniline
收率 70.0%
反应条件
详细条件
See reaction.notes.procedure_details.
后处理
- 1过滤The mixture was filtered through a bed of celite
- 2洗涤washed with dioxane
- 3其他evaporated to dryness under reduced pressure
实验过程
A solution of 4-[2-[2-ethyl-4-methyl-6-oxo-1,6-dihydro-1-pyrimidinyl]ethoxy]nitrobenzene (1.0 g, 3.3 mmol) (obtained from preparation 20) in 1,4-dioxane (20 ml) was reduced with hydrogen in the presence of 10% palladium on charcoal (100 mg) at 30 psi for 16 h. The mixture was filtered through a bed of celite and washed with dioxane and evaporated to dryness under reduced pressure to yield the title compound (625 mg, 70%).