HRID558414

反应详情

EQUATION

反应方程式

HRID 558414 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
80 °C

PROCEDURE

实验过程

N,N-Dimethylformamide (5 mL) was added to 1.0 g of polymer-supported triphenylphosphine (produced by Fluka, CAS registry number 39319-11-4) and 1.1 g of 2-fluorobenzyl bromide, and the mixture was stirred for 10 hours at 80° C. The reaction mixture was filtered, and then washed with N,N-dimethylformamide, dichloromethane, and methanol. The residue was dried under reduced pressure to prepare polymer-supported (2-fluorobenzyl)-triphenylphosphonium bromide. This product (144 mg) was added to a methanol solution (2 mL) of 30 mg of ethyl 3-formyl-4-methoxybenzoate obtained in step C of Example 1-2-1. After 80 μL of 28% sodium methoxide was added, the reactor was sealed, and the mixture was stirred for 4 hours at 70° C. The residue was diluted with ethyl acetate, washed with purified water, and dried over anhydrous sodium sulfate. The anhydrous sodium sulfate was separated by filtration, and then the filtrate was concentrated under reduced pressure. The residue was dried under reduced pressure to obtain 33 mg (80%) of ethyl 3-[2-(2-fluorophenyl)-vinyl]-4-methoxybenzoate.

WORKUP

后处理

  1. filtrationThe reaction mixture was filtered
  2. washwashed with N,N-dimethylformamide, dichloromethane, and methanol
  3. customThe residue was dried under reduced pressure
  4. customto prepare polymer-supported (2-fluorobenzyl)-triphenylphosphonium bromide
  5. customthe reactor was sealed
  6. stirringthe mixture was stirred for 4 hours at 70° C
  7. washwashed with purified water
  8. dry with materialdried over anhydrous sodium sulfate
  9. customThe anhydrous sodium sulfate was separated by filtration
  10. concentrationthe filtrate was concentrated under reduced pressure
  11. customThe residue was dried under reduced pressure