HRID2148

反应详情

EQUATION

反应方程式

HRID 2148 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To a solution of 1.50 g (6.02 mmol) of 2-[2-(2-hydroxyphenyl)vinyl]-1-methylindole, 1.89 g (7.21 mmol) of triphenylphosphine and 0.69 ml (7.22 mmol) of R-(+)-methyl lactate in 15 ml of THF was added 1.14 ml (7.24 mmol) of diethylazodicarboxylate under an ice-cooled condition, followed by stirring at room temperature for 2 hours. Brine was added to the reaction mixture, followed by extraction with methylene chloride. The extract was dried over Na2SO4, and evaporated. CHCl3 -n-hexane was added to the residue and, after filtration, the organic layer was purified by silica gel column chromatography (CHCl3 /n-hexane/AcOEt=10/10/1) to give 1.82 g (90%) of (S)-2-{2[2-(1-methoxycarbonylethoxy)phenyl]vinyl}-1-methylindole.

WORKUP

后处理

  1. temperaturecooled condition
  2. extractionfollowed by extraction with methylene chloride
  3. dry with materialThe extract was dried over Na2SO4
  4. customevaporated
  5. additionCHCl3 -n-hexane was added to the residue
  6. filtrationafter filtration
  7. customthe organic layer was purified by silica gel column chromatography (CHCl3 /n-hexane/AcOEt=10/10/1)