HRID272949

反应详情

EQUATION

反应方程式

HRID 272949 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
55 °C

PROCEDURE

实验过程

4-[4-(3-Pyrrolidin-1-yl-propoxy)-phenyl]-tetrahydro-pyran-4-carbonitrile (2 g, 6.4 mmol), diethyl dithiophosphate (15 mL, 8.9 mmol), and water (1.5 mL) were combined and stirred at ambient temperature for 5 hours, 55° C. for 2 hours then 70° C. for 2 hours. The reaction mixture was diluted with dichloromethane (100 mL) and basified to pH 8 with a saturated solution of NaHCO3 in water, and solid NaHCO3. The layers were separated, and further dichloromethane (100 mL) was used to extract the product. The combined organics were dried using Na2SO4, filtered and concentrated in vacuo to leave a yellow oil. The compound was purified with column chromatography on 50 g of silica, eluting with dichloromethane:methanol:ammonia (96:4:0.4) to dichloromethane:methanol:ammonia (90:10:1) to give a clear oil. The clear oil was dissolved in ethyl acetate (150 mL) and washed with 10% Na2CO3 solution. The organic layer was dried using Na2SO4, filtered and concentrated in vacuo to give the title compound as a white solid (0.61 g, 28%).

WORKUP

后处理

  1. wait70° C. for 2 hours
  2. customThe layers were separated
  3. extractionto extract the product
  4. customThe combined organics were dried
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customto leave a yellow oil
  8. customThe compound was purified with column chromatography on 50 g of silica
  9. washeluting with dichloromethane:methanol:ammonia (96:4:0.4) to dichloromethane:methanol:ammonia (90:10:1)
  10. customto give a clear oil
  11. washwashed with 10% Na2CO3 solution
  12. customThe organic layer was dried
  13. filtrationfiltered
  14. concentrationconcentrated in vacuo