反応式
[CH:1]1[C:13]2[CH2:12][C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[C:5]=2[CH:4]=[CH:3][CH:2]=1.S(=O)(=O)(O)O.II.[I:21](O)(=O)=O>CO>[I:21][C:9]1[CH:8]=[CH:7][C:6]2[C:5]3[C:13](=[CH:1][CH:2]=[CH:3][CH:4]=3)[CH2:12][C:11]=2[CH:10]=1参加物
6
実験手順
56.8 parts of fluorene, 200 parts of methanol, 37 parts of 63% sulfuric acid aqueous solution, 31 parts of iodine, and 34 parts of 34% iodic acid aqueous solution were stirred at 60° C. for 5 hours. After completion of the stirring, the resultant was filtrated, and it was then washed with 100 parts of water twice. Thereafter, the resultant was dried at 70° C. overnight. After completion of the drying, the resultant was recrystallized in methanol to obtain 60 parts of 2-iodofluorene in the form of white powders.
後処理
- filtrationAfter completion of the stirring, the resultant was filtrated
- washit was then washed with 100 parts of water twice
- customThereafter, the resultant was dried at 70° C. overnight
- customAfter completion of the drying, the resultant was recrystallized in methanol
出典と根拠
- ORDレコード
- ord-1d95bd822adf49d3a6d85f49bc1132eb
- 出典データセット
- uspto-grants-2014_05
- 特許番号
- US08735720B2
関連ノート
読み込み中…