HRID386033

反应详情

EQUATION

反应方程式

HRID 386033 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

n-Butyllithium (0.6 mL of 1.6M in hexanes, 0.96 mmol) was added to a cooled (−78° C.) solution of 2-bromo-6-ethynylpyridine (150 mg, 0.82 mmol) in tetrahydrofuran (4.1 mL). A tan slurry formed. The mixture was stirred for 30 minutes while warming to −30° C. at which time acetone (0.3 mL, 4.1 mmol) was added. The slurry dissolved to form a light orange solution. The reaction was stirred for an additional 2 hours while warming to 0° C. The reaction was quenched via the addition of saturated aqueous ammonium chloride and extracted with ethyl acetate (2×). The combined organics were dried over magnesium sulfate, filtered, concentrated in vacuo and purified via flash chromatography (0-50% ethyl acetate/hexanes) to afford the title compound as a white solid.

WORKUP

后处理

  1. customA tan slurry formed
  2. additionwas added
  3. dissolutionThe slurry dissolved
  4. customto form a light orange solution
  5. stirringThe reaction was stirred for an additional 2 hours
  6. customThe reaction was quenched via the addition of saturated aqueous ammonium chloride
  7. extractionextracted with ethyl acetate (2×)
  8. dry with materialThe combined organics were dried over magnesium sulfate
  9. filtrationfiltered
  10. concentrationconcentrated in vacuo
  11. custompurified via flash chromatography (0-50% ethyl acetate/hexanes)