反应 #1483123

ord-bd37c4f205544db2acadb02fb6b593e5

反应方程式

c1ccc2cc(-c3cc4c5ccccc5c5ccccc5c4c4ccccc34)ccc2c1
10-(2-naphthyl)benzo[g]chrysene
BrBr
bromine
Brc1ccc2c(c1)c1ccccc1c1cc(-c3ccc4ccccc4c3)c3ccccc3c21
3-bromo-10-(2-naphthyl)benzo[g]chrysene
收率 90.0%

反应条件

温度
100°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度the resultant was heated
  2. 2
    温度After cooling to room temperature
  3. 3
    其他Deposited solids were separated by filtration
  4. 4
    洗涤washed with water
  5. 5
    干燥with methanol, and dried
  6. 6
    其他The thus obtained solids were purified by means of silica gel column chromatography

实验过程

4.05 g of 10-(2-naphthyl)benzo[g]chrysene and 400 mL of acetic acid were placed in a flask. 1.92 g of bromine was added, and the resultant was heated with stirring at 100° C. for 8 hours. After cooling to room temperature, the reaction solution was poured to 1 L of ice water. Deposited solids were separated by filtration, and washed with water and then with methanol, and dried. The thus obtained solids were purified by means of silica gel column chromatography, whereby 4.35 g (yield: 90%) of 3-bromo-10-(2-naphthyl)benzo[g]chrysene was obtained.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08900724B2uspto-grants-2014_12