HRID2415193

反应详情

EQUATION

反应方程式

HRID 2415193 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-20 °C

PROCEDURE

实验过程

A solution of 4-(diethoxyphosphorylmethyl)-benzoic acid methyl ester (0.25 g, 0.87 mmole) in 5 mL of THF at −20° C., was treated with 0.88 mL of 1M lithium bis(trimethylsilyl)amide solution in hexanes. The mixture was stirred at −20° C. for 20 minutes before a solution of 2-(4,4-dimethyl-chroman-7-yl)-heptanal (0.16 g, 0.58 mmole) in 5 mL of THF was added. The reaction mixture was stirred at −20° C. for 30 minutes, at room temperature for 6 hours, quenched by the addition of 10 mL of saturated aqueous ammonium chloride solution and extracted with three 10 mL portions of ethyl acetate. The combined organic extracts were dried over MgSO4, filtered and concentrated in vacuo, to give a yellow oil. The product was purified by flash chromatography (SiO2, 10% ethyl acetate in hexanes) to yield 0.1 g of 4-[3-(4,4-dimethyl-chroman-7-yl)-oct-1-enyl]-benzoic acid methyl ester as a colorless oil.

WORKUP

后处理

  1. additionwas added
  2. customquenched by the addition of 10 mL of saturated aqueous ammonium chloride solution
  3. extractionextracted with three 10 mL portions of ethyl acetate
  4. dry with materialThe combined organic extracts were dried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customto give a yellow oil
  8. customThe product was purified by flash chromatography (SiO2, 10% ethyl acetate in hexanes)