HRID2116809

反应详情

EQUATION

反应方程式

HRID 2116809 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
40 °C

PROCEDURE

实验过程

2-Fluoro-N-methoxycarbonylaniline (500 mg, 3.11 mmol) was dissolved in methylene chloride (20 mL) to prepare a solution. Anhydrous aluminum chloride (986 mg, 7.77 mmol) was added to the solution, and the mixture was stirred at 40° C. for 20 min. Thereafter, the reaction solution was cooled to room temperature. A solution of isobutyl bromide (1.60 mL, 15.5 mmol) in a methylene chloride solution (6 mL) was added dropwise to the cooled reaction mixture while bubbling argon gas over a period of 10 min. The mixture was stirred for one hr. Water was added thereto, followed by separation of an organic layer. The organic layer was washed with water and was dried over anhydrous magnesium sulfate. The solvent was then removed from the dried organic layer by distillation to give 779 mg of 4-t-butyl-2-fluoro-N-methoxycarbonylaniline as a crude product. The crude product was further subjected to separation and purification by column chromatography on silica gel to give 433 mg of 4-t-butyl-2-fluoro-N-methoxycarbonylaniline (yield 64.0%, 4-t-butyl form: 5-t-butyl form=88:12).

WORKUP

后处理

  1. customto prepare a solution
  2. temperatureThereafter, the reaction solution was cooled to room temperature
  3. customwhile bubbling argon gas over a period of 10 min
  4. stirringThe mixture was stirred for one hr
  5. additionWater was added
  6. customfollowed by separation of an organic layer
  7. washThe organic layer was washed with water
  8. dry with materialwas dried over anhydrous magnesium sulfate
  9. customThe solvent was then removed from the dried organic layer by distillation