反応 #311487

ord-8f19ae6dc365494fb97bc77ebda0674a

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The mixture is evaporated
  2. 2
    その他the residue is triturated with isopropyl ether
  3. 3
    その他to provide a precipitate
  4. 4
    その他The precipitate is separated by filtration
  5. 5
    その他recrystallized from methanol

実験手順

To a solution of 2.3 g. (0.01 mole) of the product of step B in 100 ml. of chloroform is added 1.8 g. (0.02 mole) of dinitrogen tetraoxide, and the mixture is stirred at about 20° C. for 20 hours. The mixture is evaporated, and the residue is triturated with isopropyl ether to provide a precipitate. The precipitate is separated by filtration and recrystallized from methanol to provide 6,7-dihydro-2-nitro-3-phenyl-5H-indeno-[5,6-b]-furan, m.p. 161°-164° C.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US04231965uspto-grants-1980_11