反应 #451850

ord-ce45c7b70cad47a9ad9e28aa5d677ac0

反应方程式

C=CCOc1cc(-c2ccccc2)cc2ccc([N+](=O)[O-])cc12
1-Allyloxy-3-phenyl-7-nitro-naphthalene
C1CCC2CCCCC2C1
decaline
C=CCc1c(-c2ccccc2)cc2ccc([N+](=O)[O-])cc2c1O
2-Allyl-3-phenyl-7-nitro-1-naphthol

反应条件

温度
180°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度maintained under nitrogen
  2. 2
    温度After cooling
  3. 3
    其他the crystals formed
  4. 4
    洗涤were washed with petroleum ether
  5. 5
    过滤filtered off
  6. 6
    其他dried at 80° C. under reduced pressure

实验过程

31 g of 1-Allyloxy-3-phenyl-7-nitro-naphthalene prepared in step (3) were gradually heated to 180° C. in 390 ml of decaline, the solution being stirred and maintained under nitrogen. The temperature of 180° C. was maintained for about 1 hour. After cooling, the crystals formed were washed with petroleum ether, filtered off and dried at 80° C. under reduced pressure.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US04605697uspto-grants-1986_08