反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 0 °C
PROCEDURE
实验过程
To a mixture of 4-carboxy-4-methylvaleric acid p-methoxybenzyl ester (35.43 g) and triethylamine (14.14 g) in dry tetrahydrofuran (167 ml) was added dropwise a solution of ethyl chloroformate (15.23 g) in dry tetrahydrofuran (50 ml) with ice-cooling, and the mixture was stirred at 0° C. for 15 minutes. The precipitate was removed by filtration, and the filtrate was added dropwise to sodium azide (7.4 g) in water (67 ml) at a temperature up to 0° C. with stirring, followed by stirring for 30 minutes at the same temperature. The reaction mixture was diluted with benzene (200 ml) and the aqueous layer was extracted with benzene (100 ml). The combined benzene solution was washed with water, dried over anhydrous sodium sulfate and allowed to stand overnight at room temperature. After concentration to a volume of 100 to 120 ml in vacuo at a temperature below 30° C., the solution was stirred for 1 hour at 80° to 90° C. and evaporated to give an oily residue. p-Nitrobenzyl alcohol (23.32 g) and dry dioxane (22 ml) was added to the residue and the mixture was stirred for 7 hours at 120° to 130° C. and evaporated in vacuo to give an oily residue which was then purified by silica gel chromatography to give 4-methyl-4-p-nitrobenzyloxycarbonylaminovaleric acid p-methoxybenzyl ester.
WORKUP
后处理
- temperaturecooling
- customThe precipitate was removed by filtration
- additionthe filtrate was added dropwise to sodium azide (7.4 g) in water (67 ml) at a temperature up to 0° C.
- stirringwith stirring
- stirringby stirring for 30 minutes at the same temperature
- additionThe reaction mixture was diluted with benzene (200 ml)
- extractionthe aqueous layer was extracted with benzene (100 ml)
- washThe combined benzene solution was washed with water
- dry with materialdried over anhydrous sodium sulfate
- waitto stand overnight at room temperature
- concentrationAfter concentration to a volume of 100 to 120 ml in vacuo at a temperature below 30° C.
- stirringthe solution was stirred for 1 hour at 80° to 90° C.
- customevaporated
- customto give an oily residue
- stirringthe mixture was stirred for 7 hours at 120° to 130° C.
- customevaporated in vacuo
- customto give an oily residue which
- customwas then purified by silica gel chromatography