HRID8214

反应详情

EQUATION

反应方程式

HRID 8214 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

4

PROCEDURE

实验过程

A solution of 2-bromo-6-methylpyridine (0.5 g, 2.9 mmol) and (trimethylsilyl)acetylene (0.29 g, 2.9 mmol) in triethylamine (15 mL) is purged with argon. Copper(I) iodide (11 mg, 0.06 mmol) and (PPh3)2PdCl2 (42 mg, 0.06 mmol) are added and the reaction is stirred under argon at room temperature for 2 h. The solvent is removed in vacuo and the residue is diluted in ethyl acetate (50 mL) and water (50 mL). The organic is separated and washed with brine. The solvent is removed to afford a dark oil. This oil is diluted in methanol (50 mL) and treated with a 1 N sodium hydroxide solution (10 mL) and stirred for 3 h at room temperature. The aqueous is neutralized with 1 N hydrochloric acid and extracted with ethyl acetate. The solvent is removed in vacuo to afford a dark oil that is purified by SiO2 column chromatography to yield 1.16 g (24%) of the title compound as a light yellow oil.

WORKUP

后处理

  1. customThe solvent is removed in vacuo
  2. additionthe residue is diluted in ethyl acetate (50 mL)
  3. customThe organic is separated
  4. washwashed with brine
  5. customThe solvent is removed
  6. customto afford a dark oil
  7. stirringstirred for 3 h at room temperature
  8. extractionextracted with ethyl acetate
  9. customThe solvent is removed in vacuo
  10. customto afford a dark oil that
  11. customis purified by SiO2 column chromatography