反应详情

2-Methylanthraquinone (5.89 g, 0.0265 mole) and dichlorine monoxide (5.77 g, 0.0664 mole) in carbon tetrachloride (70 ml) were heated in a Carrius tube as described in Example 6 at 75° for 20.25 hrs. The product which separated as a yellow crystalline solid was dissolved in methylene chloride and filtered to separate a solid (0.49 g) judged from its infrared spectra to be anthraquinone-2-carboxylic acid. The filtrate was dried (MgSO4) and the solvent removed on a rotary evaporator to give 2-trichloromethylanthraquinone as a yellow crystalline solid (8.49 g, purity by HPLC 94.26%; yield 92.5%). An aliquot of the product was recrystallized from carbon tetrachloride and then sublimed (0.1μ) to give pure anthraquinone-2-carboxylic acid, mp 157-158.2.

1. customThe product which separated as a yellow crystalline solid
2. dissolutionwas dissolved in methylene chloride
3. filtrationfiltered
4. customto separate a solid (0.49 g)
5. dry with materialThe filtrate was dried (MgSO4)
6. customthe solvent removed on a rotary evaporator