HRID1665639

反应详情

EQUATION

反应方程式

HRID 1665639 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

A mixture of toluene (15 mL) and water (5 mL) was degassed with argon for 5 minutes. Sodium carbonate (0.80 g, 4.54 mmol) was added and the mixture was degassed with argon gas for 5 minutes. Phenyl boronic acid (0.59 g, 4.54 mmol) and 2-chloro-5-nitro-pyridine (0.6 g, 3.78 mmol) were added and the mixture was again degassed with argon gas for 5 minutes. Tetrakis palladium triphenyl phosphine (0.88 g, 0.76 mmol) was added and the mixture was degassed with argon gas for 5 minutes. The resulting mixture was heated to reflux for 3 hours. The mixture was then diluted with ethyl acetate, washed with water then brine solution. The organic layer was dried over sodium sulphate and concentrated under reduced pressure to afford a residue which was purified by column chromatography using silica gel 60-120 mesh (5% ethyl acetate in hexane) to afford 0.5 g (66%) of 5-nitro-2-phenyl-pyridine. LCMS purity: 201 (M+1)+, 98.2%, 1H NMR (DMSO-d6): δ 9.5 (s, 1H), 8.55 (dd, 1H), 8.1 (m, 2H), 7.9 (d, 1H), 7.55 (m, 3H).

WORKUP

后处理

  1. customwas degassed with argon for 5 minutes
  2. customthe mixture was degassed with argon gas for 5 minutes
  3. customthe mixture was again degassed with argon gas for 5 minutes
  4. customthe mixture was degassed with argon gas for 5 minutes
  5. temperatureThe resulting mixture was heated
  6. temperatureto reflux for 3 hours
  7. additionThe mixture was then diluted with ethyl acetate
  8. washwashed with water
  9. dry with materialThe organic layer was dried over sodium sulphate
  10. concentrationconcentrated under reduced pressure
  11. customto afford a residue which
  12. customwas purified by column chromatography