HRID1391241

反应详情

EQUATION

反应方程式

HRID 1391241 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To 1.0 g of 4-benzyloxy-2,6-diethyl-2,3,6-trimethylpiperidine (Compound 95 - prepared as described in Preparation 5) were added 0.52 g of formic acid and 1.22 g of 37% formalin at 0°-5° C. The mixture was stirred at room temperature and then refluxed by heating for 3 hours. When the reaction was complete, the reaction mixture was adjusted to a pH value of 8.0 by addition of a 5% aqueous solution of sodium bicarbonate; the mixture was then extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulphate and the solvent was removed by evaporation under reduced pressure. The residue was purified by column chromatography on silica gel using benzene as eluent; the resulting product was then distilled under reduced pressure, giving 0.6 g of Compound 100 as a pale yellow liquid (bp 132°-135° C./0.2 mmHg).

WORKUP

后处理

  1. temperaturerefluxed
  2. temperatureby heating for 3 hours
  3. extractionthe mixture was then extracted with ethyl acetate
  4. dry with materialThe extract was dried over anhydrous magnesium sulphate
  5. customthe solvent was removed by evaporation under reduced pressure
  6. customThe residue was purified by column chromatography on silica gel
  7. distillationthe resulting product was then distilled under reduced pressure