HRID392806

反应详情

EQUATION

反应方程式

HRID 392806 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

Under a nitrogen atmosphere, a solution of 2-(4-ethylphenyl)-4,4-dimethyl-2-oxazoline (1.15 g) in anhydrous tetrahydrofuran (100 mL) was cooled to −78° C. To this solution was added 1.5 M butyl lithium hexane solution (4.53 mL). After being stirred for 1 hour, 1-benzyl-4-piperidone (1.05 mL) was added dropwise. After the reaction temperature was allowed to rise up to room temperature, 2N hydrochloric acid was added to the reaction mixture to make the mixture acidic. The whole was refluxed for 2 hours. After cooling, sodium hydroxide aqueous solution was added to make the reaction mixture basic. The mixture was extracted with ethyl ether. The organic layer was washed with saturated saline solution and then dried over anhydrous Na2SO4. The concentration of the organic solvent left a residue, which was purified by column chromatography on silica gel (hexane/ethyl acetate/=3/2) to give the subject compound (409 mg).

WORKUP

后处理

  1. customto rise up to room temperature
  2. temperatureThe whole was refluxed for 2 hours
  3. temperatureAfter cooling
  4. extractionThe mixture was extracted with ethyl ether
  5. washThe organic layer was washed with saturated saline solution
  6. dry with materialdried over anhydrous Na2SO4
  7. waitThe concentration of the organic solvent left a residue, which
  8. customwas purified by column chromatography on silica gel (hexane/ethyl acetate/=3/2)