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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425342Generated: October 28, 2026

Hydrochloric Acid → 6-[(2-Methylbut-3-yn-2-yl)oxy]quinoline

https://huagongshe.com/reaction/2425342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrifluoroacetic acidHCID 6422—
Reactant2-Methyl-3-butyn-2-olHCID 8258—
Reactant6-HydroxyquinolineHCID 11374—
CatalystCuprous chlorideHCID 62652—
SolventAcetonitrileHCID 6342—
Product6-[(2-Methylbut-3-yn-2-yl)oxy]quinolineHCID 59134321—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 2-methyl-3-butyn-2-ol (2.45 mL, 25.1 mmol) and 1,8-diazabicyclo-[5.4.0]-7-undecene (4.25 mL, 28.4 mmol) in acetonitrile (15.5 mL) was stirred 0° C. for 30 minutes, and anhydrous trifluoroacetic acid (3.55 mL, 25.1 mmol) was added dropwise. The resulting mixture was added dropwise to a mixed solution of 6-hydroxyquinoline (2.43 g, 16.7 mmol), copper (I) chloride (8.3 mg, 0.0835 mmol), acetonitrile (15.5 mL) and 1,8-diazabicyclo-[5.4.0]-7-undecene (4.25 mL, 28.4 mmol) at 0° C., and stirred at 0° C. for 3 hours. The resulting solution was acidified with 1 mol/L HCl and extracted with ethyl acetate, and the resulting aqueous phase was neutralized with sodium hydrogencarbonate aqueous solution, 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=1/1 to 1/3) and the aimed product was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964623B2
Source datasetuspto-grants-2011_06
ORD IDord-1140ea18f858425baa2d397fb869d457
Source noteuspto-grants-2011_06