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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 2-Methyl-3-butyn-2-ol | HCID 8258 | — |
| Reactant | 6-Hydroxyquinoline | HCID 11374 | — |
| Catalyst | Cuprous chloride | HCID 62652 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 6-[(2-Methylbut-3-yn-2-yl)oxy]quinoline | HCID 59134321 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07964623B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-1140ea18f858425baa2d397fb869d457 |
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| Source note | uspto-grants-2011_06 |
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