HRID1493306

反应详情

EQUATION

反应方程式

HRID 1493306 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A solution of 2-chloromethyl-3,5-dicarboethoxy-4-(m-nitrophenyl)-6-methyl-1,4-dihydropyridine (5.6 g) in EtOH/DME (5/1; 20 ml) is added dropwise at +10° C. to a stirred solution of sodium thiophenate (1.8 g) in ethanol (10 ml), under N2 atmosphere. After two hours at room temperature the reaction mixture is evaporated under vacuum and the residue is partitioned between Et2O (100 ml) and water (50 ml). The organic phase is washed with a satured solution of sodium bicarbonate (2×20 ml) and water (3×20 ml), dried (Na2SO4) and evaporated to dryness. The residue is recrystallized from isopropylether to give 5.7 g of 2-(phenylthio)methyl-3,5-dicarboethoxy-4-(m-nitrophenyl)-6-methyl-1,4-dihydropyridine, m.p. 92°-94° C.

WORKUP

后处理

  1. customAfter two hours at room temperature the reaction mixture is evaporated under vacuum
  2. customthe residue is partitioned between Et2O (100 ml) and water (50 ml)
  3. washThe organic phase is washed with a satured solution of sodium bicarbonate (2×20 ml) and water (3×20 ml)
  4. dry with materialdried (Na2SO4)
  5. customevaporated to dryness
  6. customThe residue is recrystallized from isopropylether