Реакция #2383774

ord-8be9bee1de68472bb3c4776a0bed788a

Уравнение реакции

O=C1C=CC(=O)C=C1
1,4-benzoquinone
BrC(Br)c1ccccc1C(Br)Br
1,2-bis(dibromomethyl)benzene
[I-].[Na+]
sodium iodide
O=C1C=CC(=O)c2cc3ccccc3cc21
1,4-anthraquinone
Выход 47.0%

Реагенты

Нет

Растворители

Условия реакции

Температура
70°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеAfter the exothermic reaction
  2. 2
    Другоеthe formed crystals were separated by filtration
  3. 3
    Промывкаwashed with methanol and water and 23 g (the yield: 47%) of light yellow needle crystals of 1,4-anthraquinone
  4. 4
    Другоеwere obtained

Методика

In an atmosphere of argon, 60 g (550 mmole) of 1,4-benzoquinone, 100 g (240 mmole) of 1,2-bis(dibromomethyl)benzene and 235 g (1.6 mole) of sodium iodide were dissolved into 850 ml of dry dimethylformamide. After the exothermic reaction was completed, the reaction solution was heated to 70° C. and stirred for 8 hours. After the reaction was completed, the formed crystals were separated by filtration and washed with methanol and water and 23 g (the yield: 47%) of light yellow needle crystals of 1,4-anthraquinone were obtained.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06489046B1uspto-grants-2002_12