HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425338Generated: October 28, 2026
Hydrochloric Acid → 2,2,9-Trimethyl-2H-pyrano[2,3-g]quinoline
https://huagongshe.com/reaction/2425338
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl vinyl ketone | HCID 6570 | — |
| Reactant | 3-Nitrobenzenesulfonic acid | HCID 7387 | — |
| Reactant | 2,2-Dimethyl-2H-chromen-6-amine | HCID 10080881 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2,2,9-Trimethyl-2H-pyrano[2,3-g]quinoline | HCID 59134401 | 38% |
Reaction Steps
To a solution of 6-amino-2,2-dimethylchromene (10.1 g, 57.7 mmol) in ethanol (500 mL), methylvinylketone (33.0 mL, 404 mmol), m-nitrobenzenesulfonic acid (21.1 g, 104 mmol), zinc chloride (1.97 g, 14.4 mmol) and 35% hydrochloric acid (24 mL, 289 mmol) were added at room temperature and the resulting mixture was stirred at 110° C. for 5 hours. Upon the completion of the reaction, ethanol was distilled off, water was added, and the resulting solution was neutralized with sodium hydrogencarbonate and extracted with ethyl acetate. The resulting organic phase was washed with sodium chloride aqueous solution, and dried over anhydrous magnesium sulfate. After distilling off the solvent, the residue was purified by medium pressure column chromatography (hexane/ethyl acetate=3/1) and the aimed product was obtained (yield: 38%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07964623B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-55a39da3ab604a218549c99a0796ee3c |
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| Source note | uspto-grants-2011_06 |
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