HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610782Generated: October 25, 2026
Sulfuric Acid → Anthraquinone-2-aldehyde diacetate
https://huagongshe.com/reaction/1610782
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-Methylanthraquinone | HCID 6773 | — |
| Catalyst | chromium (VI) trioxide | HCID 10219390 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | Anthraquinone-2-aldehyde diacetate | HCID 86590963 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06984462B2 |
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| Source dataset | uspto-grants-2006_01 |
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| ORD ID | ord-4dacee892c4049e9beae61b6f0d1e181 |
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| Source note | uspto-grants-2006_01 |
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