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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610782Generated: October 25, 2026

Sulfuric Acid → Anthraquinone-2-aldehyde diacetate

https://huagongshe.com/reaction/1610782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant2-MethylanthraquinoneHCID 6773—
Catalystchromium (VI) trioxideHCID 10219390—
SolventAcetic AcidHCID 176—
SolventAcetic AnhydrideHCID 7918—
ProductAnthraquinone-2-aldehyde diacetateHCID 86590963—

Reaction Conditions

Temperature5 °C

Reaction Steps

To a solution of 2-methylanthraquinone (16.0 g, 72.0 mmol) in a mixture of acetic acid (400 ml) and acetic anhydride (400 ml) was added concentrated sulfuric acid (16 ml) at 5° C. Chromium trioxide (18.0 g, 0.18 mmol) was added over a period of 1 hour at 5° C. The reaction mixture was then stirred at 5° C. for 4 hours, poured into ice water, and extracted with chloroform. The organic extract was dried over MgSO4 and concentrated under vacuum to give anthraquinone-2-aldehyde diacetate (16.0 g, 65%.) To a solution of the anthraquinone-2-aldehyde diacetate (16.0 g, 47.3 mmol) in acetic acid (400 ml) was added dropwise 35% aqueous hydrochloric acid (170 ml) at room temperature. The reaction mixture had been stirred while refluxing for 15 min, cooled to room temperature, filtered off with suction, and washed with water. After drying, anthraquinone-2-aldehyde (10.0 g, 89%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06984462B2
Source datasetuspto-grants-2006_01
ORD IDord-4dacee892c4049e9beae61b6f0d1e181
Source noteuspto-grants-2006_01