HRID1252221

反应详情

EQUATION

反应方程式

HRID 1252221 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

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

  1. temperaturecooling
  2. customThe precipitate was removed by filtration
  3. additionthe filtrate was added dropwise to sodium azide (7.4 g) in water (67 ml) at a temperature up to 0° C.
  4. stirringwith stirring
  5. stirringby stirring for 30 minutes at the same temperature
  6. additionThe reaction mixture was diluted with benzene (200 ml)
  7. extractionthe aqueous layer was extracted with benzene (100 ml)
  8. washThe combined benzene solution was washed with water
  9. dry with materialdried over anhydrous sodium sulfate
  10. waitto stand overnight at room temperature
  11. concentrationAfter concentration to a volume of 100 to 120 ml in vacuo at a temperature below 30° C.
  12. stirringthe solution was stirred for 1 hour at 80° to 90° C.
  13. customevaporated
  14. customto give an oily residue
  15. stirringthe mixture was stirred for 7 hours at 120° to 130° C.
  16. customevaporated in vacuo
  17. customto give an oily residue which
  18. customwas then purified by silica gel chromatography