تفاعل #3415

ord-fb181b43b2cf48a49bb845d00e4222a4

معادلة التفاعل

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

الكواشف

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةwhile maintaining the temperature below 40° C.
  2. 2
    ترشيحThe mixture was filtered through celite
  3. 3
    استخلاصthe aqueous filtrate was extracted with EtOAc (4×)
  4. 4
    غسيلThe filter cake was washed with EtOAc
  5. 5
    تجفيفdried (MgSO4)
  6. 6
    تركيزconcentrated
  7. 7
    أخرىchromatographed (silica gel; CHCl3 /MeOH, 98:2)

الإجراء التجريبي

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)+.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05733912uspto-grants-1998_03