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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425340Generated: October 28, 2026

Hydrochloric Acid → 2,2,7-Trimethyl2H-pyrano[2,3-g]quinoline

https://huagongshe.com/reaction/2425340

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantChloranilHCID 8371—
ReactantSodium BicarbonateHCID 516892—
Reactant2,2-Dimethyl-2H-chromen-6-amineHCID 10080881—
CatalystZincchlorideHCID 3007855—
Solvent1-ButanolHCID 263—
SolventTetrahydrofuranHCID 8028—
Product2,2,7-Trimethyl2H-pyrano[2,3-g]quinolineHCID 5913439122%

Reaction Conditions

Temperature120 °C

Reaction Steps

To 6-amino-2,2-dimethylchromene (1.00 g, 5.71 mmol), 35% hydrochloric acid (1.43 mL, 17.1 mmol), p-chloranil (1.40 g, 5.71 mmol) and n-butanol (1.3 mL) were added at room temperature and the temperature was increased to 120° C. A solution of crotyl aldehyde (0.567 mL, 6.84 mmol) in n-butanol (0.52 mL) was added and the resulting mixture was stirred at 120° C. for 20 minutes. A solution of zinc chloride (0.777 g, 5.71 mmol) in tetrahydrofuran (10 mL) was added, and the resulting mixture was stirred at 120° C. for 20 minutes. Upon the completion of the reaction, sodium hydrogencarbonate aqueous solution was added, and the resulting solution was extracted with ethyl acetate and dried over anhydrous magnesium sulfate. After distilling off the solvent, the residue was purified by column chromatography (hexane/ethyl acetate=2/1), and recrystallized with ethyl acetate to obtain the aimed product (yield: 22%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964623B2
Source datasetuspto-grants-2011_06
ORD IDord-bad69238c4064d99850c0430bd4db9f9
Source noteuspto-grants-2011_06