反应 #2171031

ord-06bfcef7558e4389b6310db109e37cb3

反应方程式

Cc1ccc(N)c(N)c1
1,2-Diamino-4-methylbenzene
O=C(C(=O)c1ccccc1)c1ccccc1
benzil
Cc1ccc2nc(-c3ccccc3)c(-c3ccccc3)nc2c1
6-methyl-2,3-diphenylquinoxaline

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The solvent was evaporated in vacua
  2. 2
    其他the black residue recrystallised three times from ethanol

实验过程

1,2-Diamino-4-methylbenzene (25.0 g, 0.20 mol) and benzil (43 g, 0.20 mol) were refluxed in ethanoic acid (250 ml) overnight. The solvent was evaporated in vacua and the black residue recrystallised three times from ethanol to give pale brown crystals of 6-methyl-2,3-diphenylquinoxaline, 39.6 g, 65% (m.pt. 114.5-116° C. (lit.i 115-116° C.)). 1H NMR (CDCl3, 300 MHz) δ 8.08 (d, J 8.4 Hz, 1H, Hs of quinoxaline), 7.97 (bs, 1H, Hs of quinoxaline), 7.60 (d of d, J 8.4 Hz, J 1.8 Hz, 1H, Hs of quinoxaline), 7.50-7.58 (m, 4H, phenyl rings), 7.30-7.38 (m, 6H, phenyl rings), 2.62 (s, 3H, CH3).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US06716371B1uspto-grants-2004_04