反应 #2383775

ord-1a55eab8c8d84a5eaecd0f49749f25e5

反应方程式

O=C1C=CC(=O)c2cc3ccccc3cc21
1,4-anthraquinone
BrCc1c(C(Br)Br)ccc2ccccc12
1-(bromomethyl)-2-(dibromomethyl)naphthalene
[I-].[Na+]
sodium iodide
O=C1c2cc3ccccc3cc2C(=O)c2cc3c(ccc4ccccc43)cc21
8,15-benzo[a]pentacenequinone

反应条件

温度
70°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他After the exothermic reaction
  2. 2
    其他the formed crystals were separated by filtration
  3. 3
    洗涤washed with methanol and water and light yellow needle crystals of 8,15-benzo[a]pentacenequinone
  4. 4
    其他were obtained in the quantitative amount

实验过程

In an atmosphere of argon, 6.9 g (33 mmole) of 1,4-anthraquinone, 9.8 g (25 mmole) of 1-(bromomethyl)-2-(dibromomethyl)naphthalene and 25 g (660 mmole) of sodium iodide were dissolved into 85 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 light yellow needle crystals of 8,15-benzo[a]pentacenequinone were obtained in the quantitative amount.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US06489046B1uspto-grants-2002_12