반응 #8248

ord-0f65b8e12b144f6f95b7f3ce346cb7c1

반응 방정식

Cc1nccn1-c1ccc([N+](=O)[O-])cc1F
3-Fluoro-4-(2-methylimidazol-1-yl)nitrobenzene
O=C[O-].[NH4+]
ammonium formate
Cc1nccn1-c1ccc(N)cc1F
title compound
수율 100.1%
Cc1nccn1-c1ccc(N)cc1F
5-Amino-2-(2-methylimidazol-1-yl)fluorobenzene
수율 100.1%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도cooled to 0° under nitrogen
  2. 2
    여과filtered through celite, celite
  3. 3
    세척washed with methanol (100 ml), and filtrate
  4. 4
    기타evaporated to dryness
  5. 5
    기타The residue was partitioned between ethyl acetate (800 ml) and 10% aqueous sodium bicarbonate (250 ml)
  6. 6
    기타The organic layer was separated
  7. 7
    세척washed with brine (250 ml)
  8. 8
    건조dried (magnesium sulfate)
  9. 9
    기타evaporated

실험 절차

3-Fluoro-4-(2-methylimidazol-1-yl)nitrobenzene (40 g, 0.181 M) was dissolved in a mixture of methanol (200 ml) and tetrahydrofuran (800 ml), cooled to 0° under nitrogen, and treated with ammonium formate (57 g, 0.905 M) followed by palladium on charcoal (10%, 2 g). The mixture was stirred at ambient temperature for 18 hours, filtered through celite, celite washed with methanol (100 ml), and filtrate evaporated to dryness. The residue was partitioned between ethyl acetate (800 ml) and 10% aqueous sodium bicarbonate (250 ml). The organic layer was separated, washed with brine (250 ml), dried (magnesium sulfate) and evaporated to give title compound (34.6 g).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07087629B2uspto-grants-2006_08