反応 #2298754

ord-180ad0539e6e48ecb10c480509950b77

反応条件

温度
5°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他to separate the solution
  2. 2
    乾燥the organic layer was dried on anhydrous magnesium sulfate
  3. 3
    その他A residue obtained
  4. 4
    workup.DISTILLATIONafter distilling the solvent
  5. 5
    その他recrystallized from a mixed solvent of ethanol and ethyl acetate

実験手順

4-(4-Allyloxybutyloxy)benzoic acid 1.34 g and 2,7-dihydroxy-9-methylfluorene 0.46 g were dissolved in 30 ml of methylene chloride and cooled down to 5° C., and 0.01 g of dimethylaminopyridine and 1.15 g of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride were added thereto, followed by stirring the solution at a room temperature for 12 hours. Water 50 ml was added to separate the solution, and the organic layer was dried on anhydrous magnesium sulfate. A residue obtained after distilling the solvent off was refined by means of silica gel chromatography and recrystallized from a mixed solvent of ethanol and ethyl acetate to obtain 0.6 g of 2,7-di[4-(4-allyloxybutyloxy)benzoyloxy]-9-methylfluorene. Phase transition temperature: C 107 N 222 I

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07101595B2uspto-grants-2006_09