反应 #1104
ord-77b579259b0e47c2ac2dc691717deb93
反应方程式
HCl
4-(4-oxocyclohexylamino)-3-methoxy-2-methylpyridine
THF
magnesium
4-tert-butylbenzyl bromide
→
4-(4-Hydroxy-4-tert-butylbenzylcyclohexylamino)-3-methoxy-2-methylpyridine
溶剂
反应条件
详细条件
See reaction.notes.procedure_details.
后处理
- 1萃取the mixture is extracted several times with ethyl acetate
- 2洗涤the combined ethyl acetate phases are washed with sodium hydrogen carbonate solution
- 3其他Purification
- 4温度increasing amounts of methanol
- 5workup.ADDITIONare added
实验过程
A Grignard solution is prepared from 1.2 g of magnesium and 12.9 g of 90% strength 4-tert-butylbenzyl bromide in 100 ml of abs. ether. 2.9 g of 4-(4-oxocyclohexylamino)-3-methoxy-2-methylpyridine in 50 ml of absolute THF are added dropwise to this solution. After 17 hours at room temperature it is acidified with 25 ml of 2N HCl, the mixture is extracted several times with ethyl acetate and the combined ethyl acetate phases are washed with sodium hydrogen carbonate solution. Purification is carried out by column chromatography on silica gel using ethyl acetate to which increasing amounts of methanol are added.