HRID1387001

反应详情

EQUATION

反应方程式

HRID 1387001 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
80 °C

PROCEDURE

实验过程

A solution of methyl 4-[[trans-2-(1-piperidyl)cyclohexyl]oxy]benzoate (Part B) (2.232 g, 7.03 mmol) and 10.6 mL (10.6 mmol) of 1.0 N NaOH in 60 mL of 1:1 mixture of MeOH/THF was stirred at 80° C. for 20 h. The mixture was then cooled to room temperature, stirred for additional 7 h, and concentrated under reduced pressure. The residue was dissolved in 50 mL of 1.0 N HCl. This solution was extracted with 200 mL of EtOAc. The organic layer was washed with 200 mL of water. The combined aqueous layers were cooled to 0° C. and neutralized with 15 mL of 2.0 N NaOH. They were then concentrated under reduced pressure and the residue was taken up in 10% MeOH in CH2Cl2 and then filtered. The filtrate was concentrated and the residue was dried over P2O5 in a vacuum oven at 55° C.

WORKUP

后处理

  1. temperatureThe mixture was then cooled to room temperature
  2. stirringstirred for additional 7 h
  3. concentrationconcentrated under reduced pressure
  4. dissolutionThe residue was dissolved in 50 mL of 1.0 N HCl
  5. extractionThis solution was extracted with 200 mL of EtOAc
  6. washThe organic layer was washed with 200 mL of water
  7. temperatureThe combined aqueous layers were cooled to 0° C. and neutralized with 15 mL of 2.0 N NaOH
  8. concentrationThey were then concentrated under reduced pressure
  9. filtrationfiltered
  10. concentrationThe filtrate was concentrated
  11. dry with materialthe residue was dried over P2O5 in a vacuum oven at 55° C.