反应 #1098

反应方程式

4-(O-benzylhydroxylamino)-3-methoxy-2-methylpyridine

sodium hydride

3,3-dimethyl-9-tosyloxy-1,5-dioxaspiro[5.5]undecane

hydrogen

→

4-[O-Benzyl-N-(3,3-dimethyl-1,5-dioxaspiro[5.5]undec-9-yl)hydroxylamino]-3-methoxy-2-methylpyridine

溶剂

THF

DMSO

反应条件

后处理

1. 1
   workup.DISTILLATIONThe THF is then distilled off in vacuo
2. 2
   workup.ADDITIONthe mixture is poured into water
3. 3
   萃取After extracting with methylene chloride
4. 4
   其他the product is purified by chromatography on silica gel (ethyl acetate)

实验过程

7.3 g of 4-(O-benzylhydroxylamino)-3-methoxy-2-methylpyridine in 30 ml of absolute DMSO are deprotonated under N2 using 0.9 g of sodium hydride (80% strength). After evolution of hydrogen has ended, 11.7 g of 3,3-dimethyl-9-tosyloxy-1,5-dioxaspiro[5.5]undecane are added in 50 ml of absolute THF. The mixture is stirred at room temperature for 1 hour and at 50° C. for 4 hours. The THF is then distilled off in vacuo and the mixture is poured into water. After extracting with methylene chloride, the product is purified by chromatography on silica gel (ethyl acetate). 6.5 g=51%

来源