HRID1885373

反应详情

EQUATION

反应方程式

HRID 1885373 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

4-Bromotoluene (6 g) was dissolved in tetrahydrofuran (20 ml). To this solution at -78° C. under N2 was added over a ten minute period, 1.7M tBuLi (42 ml). After two hours at room temperature, the reaction mixture was cooled to 0° C. and 1M ZnCl2 (36 ml) was added over a ten minute period. After one half hour at room temperature, bis(triphenylphosphine)nickel(II) chloride (1.32 g) was added followed by dimethyl-2-bromo-terepthalate (6 g) in tetrahydrofuran (20 ml) dropwise over a five minute period. The reaction mixture was stirred at room temperature for two hours. The tetrahydrofuran was removed under reduced pressure. The residue was treated with ethyl acetate and 1N HCl and the layers separated. The organic phase was washed with water, brine, dried over magnesium sulfate and evaporated gave the crude product. Chromatography on silica gel using 5% hexanes/methylene chloride gave the desired product (5.33 g).

WORKUP

后处理

  1. additionTo this solution at -78° C. under N2 was added over a ten minute period
  2. waitAfter one half hour at room temperature
  3. customThe tetrahydrofuran was removed under reduced pressure
  4. additionThe residue was treated with ethyl acetate and 1N HCl
  5. customthe layers separated
  6. washThe organic phase was washed with water, brine
  7. dry with materialdried over magnesium sulfate
  8. customevaporated
  9. customgave the crude product