Hydrogen iodide → 2,6-Dibromoanthracene

HRID 556212ノート

反応式

HRID 556212 の反応式
[Br:1][C:2]1[CH:15]=[CH:14][C:13]2[C:12](=O)[C:11]3[C:6](=[CH:7][CH:8]=[C:9]([Br:17])[CH:10]=3)[C:5](=O)[C:4]=2[CH:3]=1.I.[PH2](O)=O>C(O)(=O)C>[Br:1][C:2]1[CH:15]=[CH:14][C:13]2[C:4](=[CH:5][C:6]3[C:11]([CH:12]=2)=[CH:10][C:9]([Br:17])=[CH:8][CH:7]=3)[CH:3]=1

参加物

5

反応物 3

HCID 24841Hydrogen iodideHCID 4124402Phosphinic AcidHCID 109594842,6-Dibromoanthraquinone

生成物 1

HCID 220589062,6-Dibromoanthracene

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

実験手順

Subsequently, a mixture of 2,6-dibromoanthraquinone (22.41 g, 61.23 mmol), acetic acid (250 mL), 56-58% hydriodic acid (100 mL), and 50% hypophosphorous acid (55 mL) was refluxed for 5 days. The mixture was cooled to RT and poured into ice water (800 mL). The resulting precipitate was filtered, washed with water and ethanol, and recrystallized from toluene (620 mL) to give 2,6-dibromoanthracene: 14.49 g pale yellow flake-like crystals.

後処理

  1. temperaturewas refluxed for 5 days
  2. filtrationThe resulting precipitate was filtered
  3. washwashed with water and ethanol
  4. customrecrystallized from toluene (620 mL)

出典と根拠

ORDレコード
ord-3a0936236e994d7e8cc92e93c6d99c85
出典データセット
uspto-grants-2011_11
特許番号
US08053840B2

反応ノート

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