HRID2078345

反应详情

EQUATION

反应方程式

HRID 2078345 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

4

CONDITIONS

反应条件

温度
55 °C

PROCEDURE

实验过程

A mixture of ethyl 4-(2-bromoethoxy)-2-(2-chloro-6-iodophenyl)butanoate (5.8 g, 12 mmol) and TEA (15 mL, 110 mmol) in 24 mL ACN was degassed by vacuum and back filled with nitrogen 3 times. The mixture was treated with 3,3,3-triethoxyprop-1-yne (2.7 g, 16 mmol), dichlorobis(triphenylphosphine)palladium(ii) (0.17 g, 0.24 mmol) and copper(I) iodide (0.12 g, 0.61 mmol). The mixture was stirred at 55° C. for 2 hours. The mixture was cooled to room temperature, diluted with 100 mL EtOAc, and washed with water (3×20 mL) and then with 20 mL saturated NaCl. The organic layers were dried and concentrated. The crude product was evaporated from 50 mL toluene and dissolved in 50 mL DMF. The mixture was treated with 0.7 g NaH. The mixture was stirred at room temperature for 15 hours. The mixture was quenched with 50 mL water and neutralized with 10% HCl to pH=5. The mixture was then extracted with ether (3×100 mL). The combined organic layers were washed with water (3×20 mL) and saturated NaCl (20 mL), and then dried over anhydrous sodium sulfate and concentrated. The crude product was purified by column chromatography (10% EtOAc/hexane) to give 2.42 g yellow oil. MS m/e: (M+H)+ 487.

WORKUP

后处理

  1. customwas degassed by vacuum
  2. additionback filled with nitrogen 3 times
  3. temperatureThe mixture was cooled to room temperature
  4. washwashed with water (3×20 mL)
  5. customThe organic layers were dried
  6. concentrationconcentrated
  7. customThe crude product was evaporated from 50 mL toluene
  8. dissolutiondissolved in 50 mL DMF
  9. additionThe mixture was treated with 0.7 g NaH
  10. stirringThe mixture was stirred at room temperature for 15 hours
  11. customThe mixture was quenched with 50 mL water and neutralized with 10% HCl to pH=5
  12. extractionThe mixture was then extracted with ether (3×100 mL)
  13. washThe combined organic layers were washed with water (3×20 mL) and saturated NaCl (20 mL)
  14. dry with materialdried over anhydrous sodium sulfate
  15. concentrationconcentrated
  16. customThe crude product was purified by column chromatography (10% EtOAc/hexane)