HRID1879281

反应详情

EQUATION

反应方程式

HRID 1879281 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-30 °C

PROCEDURE

实验过程

Ethyl 3-piperidin-1-ylacrylate (94%, 9.4 g, 48 mmol) was initially charged in toluene (100 ml) and cooled to −30° C. At this temperature, difluoroacetyl fluoride (5.0 g, 51 mmol) was introduced. Tributylamine (9.5 g, 51 mmol) was then added to the reaction mixture. The reaction mixture was stirred at −30° C. for 3 h and then, over a period of 1 hour, warmed to room temperature. The reaction mixture was washed with deionized water (50 ml). After separation of the phases, the aqueous phase was extracted once with toluene (100 ml). The toluene phases were combined and washed with an aqueous saturated NaCl solution (100 ml) and the solvent was then removed under reduced pressure. This gave ethyl 4,4-difluoro-3-oxo-2-(1-piperidin-1-ylmethylidene)butyrate as an orange oil (amount: 12.7 g; purity according to GC: 82.15%; yield: 82.8%).

WORKUP

后处理

  1. waitover a period of 1 hour
  2. temperaturewarmed to room temperature
  3. washThe reaction mixture was washed with deionized water (50 ml)
  4. customAfter separation of the phases
  5. extractionthe aqueous phase was extracted once with toluene (100 ml)
  6. washwashed with an aqueous saturated NaCl solution (100 ml)
  7. customthe solvent was then removed under reduced pressure