HRID2122098

反应详情

EQUATION

反应方程式

HRID 2122098 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

4

CONDITIONS

反应条件

温度
100 °C

PROCEDURE

实验过程

The metathesis product from above was oxidized to the epoxide as described by Bach et al. in “Epoxidation of Olefins by Hydrogen peroxide-Acetonitrile: cis-Cyclohexene Oxide”, Organic synthesis collective Volume Vii, 1990, p. 126 or with m-chloroperoxybenzoic acid. The glyceride esters were hydrolyzed and the epoxide opened to the diol by warming the epoxide in 2 M KOH and 20 mL of isopropyl alcohol (IPA) to 60° C. for six hours. The solution was concentrated and washed with 50 mL of 1 M HCl. The organic phase was dried with anhydrous sodium sulfate, filtered and used in the next reaction without further purification. Lactonization was accomplished using the following procedure: the crude diol (2.9 g, 9.0 mmol) was dissolved into 50 mL of anhydrous toluene containing 50 mg of toluenesulfonic acid and heated to 100° C. for six hours. The mixture was cooled to room temp and washed with 50 mL of NaHCO3 saturated water. The organic phase was dried with anhydrous sodium sulfate, filtered and used in the next reaction without further purification. The dried solution was acetylated with 1.8 g (0.018 mmol) acetic anhydride and 5 mL of triethylamine. The solution was stirred at room temp overnight. The reaction was worked up by washing with 50 mL of 1 M HCl and 50 mL wash of NaHCO3 saturated water. The organic phase was dried with anhydrous sodium sulfate, filtered, concentrated and to yield (5R,6S)-6-acetoxy-5-hexadecanolide and its stereoisomers, and then purified by column chromatography.

WORKUP

后处理

  1. concentrationThe solution was concentrated
  2. washwashed with 50 mL of 1 M HCl
  3. dry with materialThe organic phase was dried with anhydrous sodium sulfate
  4. filtrationfiltered
  5. customused in the next reaction without further purification
  6. temperatureThe mixture was cooled to room temp
  7. washwashed with 50 mL of NaHCO3 saturated water
  8. dry with materialThe organic phase was dried with anhydrous sodium sulfate
  9. filtrationfiltered
  10. customused in the next reaction without further purification
  11. washby washing with 50 mL of 1 M HCl and 50 mL
  12. washwash of NaHCO3 saturated water
  13. dry with materialThe organic phase was dried with anhydrous sodium sulfate
  14. filtrationfiltered
  15. concentrationconcentrated