HRID20014

反应详情

EQUATION

反应方程式

HRID 20014 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-78 °C

PROCEDURE

实验过程

To a solution of 5-(methoxymethoxy)-2-neopentylpyridine (16.5 g, 79 mmol) and in THF (200 mL) −78° C. is added tert-butyllithium (46 ml, 79 mmol) (1.7 M in pentane ) over 2 min via cannula. The reaction was stirred at −78° C. 30 min, and acetaldehyde (11 ml, 197 mmol) was added. The reaction was stirred at −78° C. 10 min, then the reaction was warmed to rt and stirred 3 h. The reaction was quenched by addition of saturated aqueous NH4Cl (400 mL), extracted with EtOAc (3×200 mL), the combined organic layers washed with saturated NaCl (10 mL), dried (Na2SO4), and concentrated to give a orange oil, which was purified by chromatography on an ISCO (330 g SiO2, 10%-50% EtOAc/Hexane) gives 1-(5-(methoxymethoxy)-2-neopentylpyridin-4-yl)ethanol as a clear, light yellow oil.

WORKUP

后处理

  1. stirringThe reaction was stirred at −78° C
  2. temperature10 min, then the reaction was warmed to rt
  3. stirringstirred 3 h
  4. customThe reaction was quenched by addition of saturated aqueous NH4Cl (400 mL)
  5. extractionextracted with EtOAc (3×200 mL)
  6. washthe combined organic layers washed with saturated NaCl (10 mL)
  7. dry with materialdried (Na2SO4)
  8. concentrationconcentrated
  9. customto give a orange oil, which
  10. customwas purified by chromatography on an ISCO (330 g SiO2, 10%-50% EtOAc/Hexane)