참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Carbon Tetrachloride | HCID 5943 | — |
| 반응물 | 2-Methylanthraquinone | HCID 6773 | — |
| 반응물 | Chlorine monoxide | HCID 24646 | — |
| 생성물 | 2-Trichloromethylanthraquinone | HCID 23337645 | 92.5% |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04226783 |
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| 출처 데이터셋 | uspto-grants-1980_10 |
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| ORD ID | ord-c3d02c9386594155828c4f1f3dcf0bb0 |
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| 출처 메모 | uspto-grants-1980_10 |
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