HRID2621

反应详情

EQUATION

反应方程式

HRID 2621 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

4

PROCEDURE

实验过程

To a cold (-78° C.) solution of ethyl 4-(diethoxyphosphoryl-3,3-dimethoxypropyl)benzoate (Compound D, 690 mg, 1.75 mmol) in THF (8 mL) was added n-BuLi in hexane (1.6M solution, 1.1 mL). The mixture was gradually warmed to ambient temperature over 30 min and stirred for 5 minutes. The mixture was recooled to -78° C. and 2,2-dimethyl-4(5-methyl-thien-2-yl)-chrom-3-en-6-al (Compound S, 300 mg, 1.1 mmol) in THF (1 mL) was added to the reaction mixture. The mixture was stirred at ambient temperature for 2 hours. The reaction mixture was diluted with ethyl acetate (100 mL) and washed with brine (10 mL) dried and the solvent was removed by evaporation. The material was subjected to flash chromatography on silica gel to obtain the E and Z olefinic compounds, which were dissolved in dichloromethane (5 mL) and cooled to -78° C. A solution of SnCl4 in dichloromethane (52 mg in 0.2 mL) was added to the olefinic compounds. The resulting mixture was stirred for 30 minutes, quenched with methanol, water and diluted with ethyl acetate (100 mL). The organic layer was washed with brine and dried. Solvent was removed under reduced pressure and purified by silicagel chromatography to afford the title compound as a white solid.

WORKUP

后处理

  1. customwas recooled to -78° C.
  2. stirringThe mixture was stirred at ambient temperature for 2 hours
  3. washwashed with brine (10 mL)
  4. customdried
  5. customthe solvent was removed by evaporation
  6. customto obtain the E and Z olefinic compounds, which
  7. temperaturecooled to -78° C
  8. stirringThe resulting mixture was stirred for 30 minutes
  9. customquenched with methanol, water
  10. additiondiluted with ethyl acetate (100 mL)
  11. washThe organic layer was washed with brine
  12. customdried
  13. customSolvent was removed under reduced pressure
  14. custompurified by silicagel chromatography