HRID1728133

反应详情

EQUATION

反应方程式

HRID 1728133 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

To a solution of 5-iodo-2-methyl benzoic acid (24 g, 91 mmol) (AKSCI) in anhydrous tetrahydrofuran (100 mL) at 0° C. was added borane tetrahydrofuran (1 M, 250 mL, 250 mmol) dropwise. The reaction mixture was then stirred at room temperature for 2 h. The mixture was concentrated and residue was partitioned between ethyl acetate and water. Organic layer was separated, washed with brine, dried over MgSO4, and concentrated to give an off-white solid. The solid was dissolved into dichloromethane (300 mL), and activated MnO2 (20 g) was added. The mixture was then heated at reflux for 4 h, cooled to room temperature, and filtered through a short pad of celite. The filtrated was concentrated and purified by chromatography (EtOAc:hexanes=1;8) to give 5-Iodo-2-methyl-benzaldehyde as an off-white solid (Yield 5.5 g, 25%).

WORKUP

后处理

  1. concentrationThe mixture was concentrated
  2. customresidue was partitioned between ethyl acetate and water
  3. customOrganic layer was separated
  4. washwashed with brine
  5. dry with materialdried over MgSO4
  6. concentrationconcentrated
  7. customto give an off-white solid
  8. additionwas added
  9. temperatureThe mixture was then heated
  10. temperatureat reflux for 4 h
  11. temperaturecooled to room temperature
  12. filtrationfiltered through a short pad of celite
  13. concentrationThe filtrated was concentrated
  14. custompurified by chromatography (EtOAc:hexanes=1;8)