Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993459Generated: November 2, 2026

Hydrochloric Acid → 2,2,9-Trimethyl-2H-pyrano[2,3-g]quinoline

https://huagongshe.com/reaction/1993459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl vinyl ketoneHCID 6570—
Reactant3-Nitrobenzenesulfonic acidHCID 7387—
Reactant2,2-Dimethyl-2H-chromen-6-amineHCID 10080881—
CatalystZincchlorideHCID 3007855—
SolventEthanolHCID 702—
Product2,2,9-Trimethyl-2H-pyrano[2,3-g]quinolineHCID 5913440138%

Reaction Conditions

Temperature110 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652008B2
Source datasetuspto-grants-2010_01
ORD IDord-038ab670949a4e65a302824d36d5fe09
Source noteuspto-grants-2010_01