反応 #81998

ord-2191fc2787b34c36a682446433b355fc

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度to reflux
  2. 2
    抽出the solution extracted with 3×10 mL Et2O
  3. 3
    workup.ADDITIONtreated with activated charcoal
  4. 4
    乾燥dried (MgSO4)
  5. 5
    ろ過filtered through a pad of Celite
  6. 6
    その他The solvent was evaporated at reduced pressure

実験手順

4,5-Difluoro-1,2-diaminobenzene was prepared using an adaptation of the method of Tsuji et al., (Tsuji, Y. et al., J. Org. Chem. 55: 580 (1990)). Zn powder (942 mg, 14.4 mmol), CaCl2 (94.4 mg), H2O (1.0 mL) and 4.0 mL EtOH were combined and brought to reflux as described for 4-fluoro-1,2-diaminobenzene (see Example 11) and to this mixture was added slowly dropwise a solution of 4,5-difluoro-2-nitroaniline (200 mg, 1.15 mmol) in 2 mL EtOH. Analysis and workup were as described for 4-fluoro-1,2-diaminobenzene (Example 11 ) except that the reaction was dissolved in 5 mL H2O and the solution extracted with 3×10 mL Et2O. The organic layers were combined and treated with activated charcoal, dried (MgSO4) and filtered through a pad of Celite. The solvent was evaporated at reduced pressure to yield 111.5 mg (67.3%) of a brown crystalline solid. 1H NMR (CDCl3) δ 3.34 (br s, 4H, NH2), 6.53 (t, 2H, ArH).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05620979uspto-grants-1997_04