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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582849Generated: October 30, 2026

Hydrochloric Acid → HCID 21982878, compound

https://huagongshe.com/reaction/1582849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-BromotolueneHCID 7805—
Reactant2-ChloroanthraquinoneHCID 8553—
ReactantStannous chloride dihydrateHCID 61436—
ReactantMagnesiumHCID 5462224—
SolventAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21982878HCID 2198287878.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06740263B2
Source datasetuspto-grants-2004_05
ORD IDord-4f1c0bf3284841d19b111c5de4e38287
Source noteuspto-grants-2004_05