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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993462Generated: October 31, 2026

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

https://huagongshe.com/reaction/1993462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Methyl-3-butyn-2-olHCID 8258—
ReactantTrifluoroacetic anhydrideHCID 9845—
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 trifluoroacetic anhydride (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 aqueous sodium hydrogencarbonate 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 numberUS07652008B2
Source datasetuspto-grants-2010_01
ORD IDord-e07138dbbd1f4588ad721d52a1366e0f
Source noteuspto-grants-2010_01