HRID1415277

反应详情

EQUATION

反应方程式

HRID 1415277 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

1 g of homoveratric acid is dissolved in 15 ml of absolute tetrahydrofuran and treated wih 0.15 g of triethylamine. 0.72 g of chloroformic acid isobutyl ester are then slowly added dropwise at 0°-5° C and the mixture is stirred for 1 hour at 5°-10° C. There is then added dropwise a solution of 1.63 g of 2-(3,4-dimethoxyphenyl)-N-methyl-m-dithiane-2-propylamine [prepared in a manner analogous to that described in Example 15 from 2-(γ-chloropropyl)-2-(3,4-dimethoxyphenyl)-m-dithiane and methylamine] in 5 ml of tetrahydrofuran. The resulting mixture is left to stand at room temperature overnight. After evaporation of the solvent, the residue is partitioned between 1-M hydrochloric acid and ether. The organic extracts are washed with 5% sodium carbonate solution and water. After drying over magnesium sulphate, the solvent is removed by evaporation. The oily residue (1.5g) is dissolved in 15 ml of tetrahydrofuran and added dropwise to a suspension of 0.15 g of lithium aluminium hydride under reflux and under argon. The mixture is boiled for 2 hours and then treated slowly with a concentrated sodium sulphate solution in water and then with 10 ml of methylene chloride. The mixture is filtered under suction and then concentrated. The residue is chromatographed on silica gel and there is obtained N-(3,4-dimethoxyphenethyl)-2-(3,4-dimethoxyphenyl)-N-methyl-m-dithiane-2-propylamine in the form of a thick oil.

WORKUP

后处理

  1. customprepared in a manner analogous to
  2. waitThe resulting mixture is left
  3. waitto stand at room temperature overnight
  4. customAfter evaporation of the solvent
  5. customthe residue is partitioned between 1-M hydrochloric acid and ether
  6. washThe organic extracts are washed with 5% sodium carbonate solution and water
  7. dry with materialAfter drying over magnesium sulphate
  8. customthe solvent is removed by evaporation
  9. dissolutionThe oily residue (1.5g) is dissolved in 15 ml of tetrahydrofuran
  10. additionadded dropwise to a suspension of 0.15 g of lithium aluminium hydride
  11. temperatureunder reflux and under argon
  12. waitThe mixture is boiled for 2 hours
  13. additiontreated slowly with a concentrated sodium sulphate solution in water
  14. filtrationThe mixture is filtered under suction
  15. concentrationconcentrated
  16. customThe residue is chromatographed on silica gel