HRID1445334

反应详情

EQUATION

反应方程式

HRID 1445334 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
22 °C

PROCEDURE

实验过程

860 mg of 3-benzyloxy-5-isopropyl-N-methoxy-N-methylthiophene-2-carboxamide were dissolved in 50 ml of tetrahydrofuran (THF) and cooled to 0> C. in an ice bath, and 31.3 ml of 0.5 molar 4-methoxyphenymagnesium bromide solution in tetrahydrofuran were added. After 30 min, the ice bath was removed and the reaction mixture was warmed to 22° C. After one hour, 70 ml of saturated sodium bicarbonate solution were added to the reaction mixture, and it was extracted twice with 100 ml of methyl acetate each time. The combined organic phases were washed with 70 ml of saturated sodium chloride solution, dried over sodium sulfate and concentrated. The crude product was purified by column chromatography (SiO2, ethyl acetate/n-heptane=1:3).

WORKUP

后处理

  1. temperaturecooled to 0> C
  2. customthe ice bath was removed
  3. waitAfter one hour
  4. addition70 ml of saturated sodium bicarbonate solution were added to the reaction mixture, and it
  5. extractionwas extracted twice with 100 ml of methyl acetate each time
  6. washThe combined organic phases were washed with 70 ml of saturated sodium chloride solution
  7. dry with materialdried over sodium sulfate
  8. concentrationconcentrated
  9. customThe crude product was purified by column chromatography (SiO2, ethyl acetate/n-heptane=1:3)