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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993460Generated: October 27, 2026

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

https://huagongshe.com/reaction/1993460

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, aqueous sodium hydrogencarbonate 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 from ethyl acetate to obtain the aimed product (yield: 22%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652008B2
Source datasetuspto-grants-2010_01
ORD IDord-3dffc891d8fb43fab07e5cefe2e1d3a5
Source noteuspto-grants-2010_01