HRID751432

反应详情

EQUATION

反应方程式

HRID 751432 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-60 °C

PROCEDURE

实验过程

To a solution of 3-Bromo-5-methoxypyridine (2.5 g, 13.3 mmol) in anhydrous diethyl ether cooled to −100° C. was added n-butyllithium (2.5M soln in hexanes: 5.85 mL, 14.6 mmol) dropwise whilst maintaining an internal temperature <−94° C. After subsequent stirring for 30 minutes, anhydrous DMF (1.34 mL, 17.3 mmol) was added and the reaction mixture allowed to warm to −60° C.. The solution was then poured into sat'd. aq. NaCl soln. and extracted with diethyl ether (3×100 mL), the ethereal phase dried (K2CO3), filtered and evaporated in vacuo. The residue was purified on silica gel eluting with a gradient of 0 to 30% EtOAc in hexanes to afford the title material as an oil.

WORKUP

后处理

  1. temperature5.85 mL, 14.6 mmol) dropwise whilst maintaining an internal temperature <−94° C
  2. additionThe solution was then poured into sat'd
  3. extractionand extracted with diethyl ether (3×100 mL)
  4. dry with materialthe ethereal phase dried (K2CO3)
  5. filtrationfiltered
  6. customevaporated in vacuo
  7. customThe residue was purified on silica gel eluting with a gradient of 0 to 30% EtOAc in hexanes