反应 #3415

ord-fb181b43b2cf48a49bb845d00e4222a4

反应方程式

Cc1cc([N+](=O)[O-])cnc1Cl
2-Chloro-3-methyl-5-nitropyridine
Cc1cc(N)cnc1Cl
solid
收率 89.0%
Cc1cc(N)cnc1Cl
5-Amino-2-chloro-3-methylpyridine
收率 89.0%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度while maintaining the temperature below 40° C.
  2. 2
    过滤The mixture was filtered through celite
  3. 3
    萃取the aqueous filtrate was extracted with EtOAc (4×)
  4. 4
    洗涤The filter cake was washed with EtOAc
  5. 5
    干燥dried (MgSO4)
  6. 6
    浓缩concentrated
  7. 7
    其他chromatographed (silica gel; CHCl3 /MeOH, 98:2)

实验过程

2-Chloro-3-methyl-5-nitropyridine (15 g, 86.9 mmol; from Maybridge Chemical Co.) was dissolved in a solution of H2O/AcOH (5:1, 60 mL). Iron powder was added to the reaction mixture while maintaining the temperature below 40° C., and the mixture was stirred for 5 hours. The mixture was filtered through celite and the aqueous filtrate was extracted with EtOAc (4×). The filter cake was washed with EtOAc, and the EtOAc solutions were combined, dried (MgSO4), concentrated and chromatographed (silica gel; CHCl3 /MeOH, 98:2) to afford an orange solid (2.3 g, 89%): 1H NMR (CD3OD, 300 MHz) δ2.25 (s, 3H), 7.01 (d, J=2.0 Hz, 1H), 7.58 (d, J=2.0 Hz, 1H); MS (CI/NH3) m/z: 243/245 (M+H)+.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05733912uspto-grants-1998_03