HRID1837765

反应详情

EQUATION

反应方程式

HRID 1837765 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

786 mg of diethyl 2-(cyclopentyloxy)benzylphosphonate was dissolved in 10 ml of tetrahydrofuran. To the mixture was added 281 mg of potassium tert-butoxide, followed by stirring for 15 minutes under ice-cooling. A solution of 500 mg of 1-[(2-methoxy-3-pyridinyl)methyl]-4-piperidinecarboxaldehyde dissolved in 3 ml of tetrahydrofuran was added dropwise thereinto, followed by stirring at room temperature for 2 hours. Ice water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and brine, and then dried over anhydrous magnesium sulfate. The solvent was evaporated, and the resulting crude product was purified by silica gel column chromatography (n-hexane:ethyl acetate=1:1), to give 473 mg of the title compound as a pale yellow oil.

WORKUP

后处理

  1. temperaturecooling
  2. additionwas added dropwise
  3. stirringby stirring at room temperature for 2 hours
  4. extractionthe mixture was extracted with ethyl acetate
  5. washThe organic layer was washed with water and brine
  6. dry with materialdried over anhydrous magnesium sulfate
  7. customThe solvent was evaporated
  8. customthe resulting crude product was purified by silica gel column chromatography (n-hexane:ethyl acetate=1:1)