HRID394909

反应详情

EQUATION

反应方程式

HRID 394909 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
60 °C

PROCEDURE

实验过程

At room temperature, a three-neck flask equipped with a reflux condenser, internal thermometer, dropping funnel and stirrer under nitrogen protective gas was initially charged with 7.6 g of zinc powder (115 mmol) in 45 ml of isopropyl acetate. After 1.83 ml of trimethylchlorosilane (14 mmol) had been added, the mixture was heated to 60° C. for 15 min, then allowed to cool to 55° C. and 16.3 g of undiluted methyl bromoacetate (107 mmol) were subsequently added dropwise within 5 min, and the temperature was maintained at 60° C. by external cooling. The mixture was then stirred at 50° C. for 15 min. After cooling to 30° C., 9.4 g of undiluted benzaldehyde (89 mmol) were added, and the temperature was maintained at 40° C. by external cooling. After stirring had been continued at 40° C. for 30 min, the mixture was cooled to 0° C., acidified with 20 ml of 20% hydrochloric acid to a pH of 1 and the mixture was stirred for 30 min, during which excess zinc dissolved. The organic phase was then removed. The organic phase was then stirred with 30 ml of concentrated ammonia solution at 0° C. for 10 min. After the phase separation, drying was effected over sodium sulfate and the solvent was distilled off under reduced pressure. Methyl 3-hydroxy-3-phenylpropionate was obtained in a yield of 14.3 g (89% of theory) and had a boiling point of 78° C. (0.08 mbar).

WORKUP

后处理

  1. customAt room temperature, a three-neck flask equipped with a reflux condenser
  2. temperatureto cool to 55° C.
  3. temperaturethe temperature was maintained at 60° C. by external cooling
  4. temperatureAfter cooling to 30° C.
  5. temperaturethe temperature was maintained at 40° C. by external cooling
  6. stirringAfter stirring
  7. waithad been continued at 40° C. for 30 min
  8. temperaturethe mixture was cooled to 0° C.
  9. dissolutiondissolved
  10. customThe organic phase was then removed
  11. stirringThe organic phase was then stirred with 30 ml of concentrated ammonia solution at 0° C. for 10 min
  12. customAfter the phase separation
  13. customdrying
  14. distillationthe solvent was distilled off under reduced pressure