HRID57917

反应详情

EQUATION

反应方程式

HRID 57917 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

To Diisopropylamine (22.001 mmol; 2240 mg; 3.13 mL) in THF (40 mL) at 0° C. was added N-Butyllithium (2.5 mol/L) in Hexane (24.001 mmol; 9.6 mL). The reaction was stirred at 0° C. for 0.5 h, and then cooled to −78° C. 2-bromo-6-fluoro-pyridine (20.001 mmol; 3520.0 mg) in THF (10 mL) was added dropwise. The mixture was stirred at −78° C. for 2.5 h. Paraformaldehyde (40.002 mmol; 3603.3 mg) was added rapidly. The mixture was allowed to warm to room temperature and stirred overnight. The reaction was quenched with water. The layers were separated. The aqueous layer was extracted with EtOAc. The combined organic layers were concentrated and the residue was purified on silica eluted with 0 to 50% EtOAc in Heptane to afford (6-bromo-2-fluoro-3-pyridyl)methanol (1.4888 g, 36%).

WORKUP

后处理

  1. temperaturecooled to −78° C
  2. stirringThe mixture was stirred at −78° C. for 2.5 h
  3. temperatureto warm to room temperature
  4. stirringstirred overnight
  5. customThe reaction was quenched with water
  6. customThe layers were separated
  7. extractionThe aqueous layer was extracted with EtOAc
  8. concentrationThe combined organic layers were concentrated
  9. customthe residue was purified on silica
  10. washeluted with 0 to 50% EtOAc in Heptane