HRID423027

反应详情

EQUATION

反应方程式

HRID 423027 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

A solution of LDA (107 ml, 214.01 mmol) was added to a stirred solution of tert-butyl 4-cyanopiperidine-1-carboxylate (30 g, 143 mmol) in THF (250 ml) at −78° C., under nitrogen. The resulting solution was stirred at −78° C. for 30 minutes. Ethyl chloroformate (16.37 ml, 171.2 mmol) was added. The resulting solution was stirred and allowed to warm to room temperature. The reaction mixture was quenched with saturated NaHCO3 (250 ml), extracted with DCM, and the organic layer was washed with saturated brine (100 ml) then dried over MgSO4, filtered and evaporated to afford the crude material as a orange oil. This material was purified by flash silica chromatography, elution gradient 10% EtOAc in isohexane. Pure fractions were evaporated to dryness to afford 1-tert-butyl 4-ethyl 4-cyanopiperidine-1,4-dicarboxylate (20.8 g, 51.6%) as a yellow oil.

WORKUP

后处理

  1. stirringThe resulting solution was stirred
  2. temperatureto warm to room temperature
  3. customThe reaction mixture was quenched with saturated NaHCO3 (250 ml)
  4. extractionextracted with DCM
  5. washthe organic layer was washed with saturated brine (100 ml)
  6. dry with materialthen dried over MgSO4
  7. filtrationfiltered
  8. customevaporated
  9. customto afford the crude material as a orange oil
  10. customThis material was purified by flash silica chromatography, elution gradient 10% EtOAc in isohexane
  11. customPure fractions were evaporated to dryness