HRID868445

反应详情

EQUATION

反应方程式

HRID 868445 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

2.61 g (6.0 mmole) of 2-benzyloxy-3-octadecyloxypropanol was dissolved in 20 ml of chloroform freed of ethanol, and 3.03 g (30.0 mmole, 5.0 eq) of dry triethylamine was added to the mixture with stirring under ice-cooling. Then, 970 mg (6.3 mmole, 1.05 eq) of phosphorus oxychloride dissolved in 40 ml of chloroform freed of ethanol was added to the mixture. The resulting mixture was stirred at 0° C. for 30 minutes and at room temperature for 1 hour. Then, the mixture was cooled to 0° C. and 2.80 g (7.8 mmole, 1.3 eq) of 8-trimethylammoniooctanol monotosylate suspended in 60 ml of dry pyridine was dropwise added thereto over a period of 20 minutes. The mixture was stirred at 0° C. for 1 hour and at room temperature for 3 days. 50 ml of an aqueous solution saturated with sodium hydrogencarbonate was added the reaction mixture, which was concentrated to dryness under reduced pressure. The residue was purified by column chromatography on Amberlite resin (30 ml of IR-120, 15 ml of IR-410; eluent: 95% tetrahydrofuran).

WORKUP

后处理

  1. additionwas added to the mixture
  2. temperaturecooling
  3. additionwas added to the mixture
  4. stirringThe resulting mixture was stirred at 0° C. for 30 minutes and at room temperature for 1 hour
  5. additionwas dropwise added
  6. stirringThe mixture was stirred at 0° C. for 1 hour and at room temperature for 3 days
  7. concentrationwas concentrated to dryness under reduced pressure
  8. customThe residue was purified by column chromatography on Amberlite resin (30 ml of IR-120, 15 ml of IR-410; eluent: 95% tetrahydrofuran)