Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Bromotoluene | HCID 7805 | — |
| Reactant | 2-Chloroanthraquinone | HCID 8553 | — |
| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21982878 | HCID 21982878 | 78.1% |
Reaction Steps
213.8 g of 4-bromotoluene dissolved in anhydrous THF(200 ml) was slowly added to 32.6 g of magnesium in 500 ml of anhydrous THF for 2 hours. The mixed solution was refluxed for 3 hours, and then cooled to room temperature. 121 g of 2-chloroanthraquinone was added to cooled solution. The resulting solution was stirred for 3 hours, and then refluxed for 3 hours. Then, 400 ml of 10% aqueous hydrochloric acid solution was added to the resulting solution. An organic layer was separated from the solution. The resulting solvent was distilled under a vacuum, by which a brown solution was obtained. 500 ml of Glacial acetic acid and 100 g of SnCl2.2H2O were added to the brown solution. The mixed solution was stirred at room temperature for 1 hour, heated for 3 hours and refluxed. The solution was further stirred at room temperature for 3 hours. Thus, a pale yellow product was obtained. This product was recrystallized using glacial acetic acid. In this way, a pure product was obtained in the form of pale yellow crystals(153 g, m.p. 202-203.5° C., yield 78%). Results of 1H NMR(200 MHz, CDCl3) and IR(KBr) for the obtained compound are described in the following Table 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06740263B2 |
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| Source dataset | uspto-grants-2004_05 |
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| ORD ID | ord-4f1c0bf3284841d19b111c5de4e38287 |
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| Source note | uspto-grants-2004_05 |
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