HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70524Generated: October 29, 2026
Water → 3-(5-Chloro-6-methoxypyridin-2-yl)prop-2-yn-1-ol
https://huagongshe.com/reaction/70524
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Propargyl alcohol | HCID 7859 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 6-Bromo-3-chloro-2-methoxypyridine | HCID 58452302 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-(5-Chloro-6-methoxypyridin-2-yl)prop-2-yn-1-ol | HCID 58452667 | 80% |
Reaction Steps
Triethylamine (70 mL) and bistriphenylphosphinepalladium(II) dichloride (756 mg) were added to 6-bromo-3-chloro-2-methoxypyridine (12.1 g), 2-propyn-1-ol (4.0 g) and copper iodide (210 mg) in a nitrogen atmosphere, and the mixture was stirred at room temperature for four hours. Water and ethyl acetate were added to the reaction solution, followed by filtration. The aqueous layer was adjusted to pH 3 or less with 1 M hydrochloric acid, followed by extraction with ethyl acetate. The organic layer was washed with brine and dried over sodium sulfate. After filtration, the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=7:3→5:5) to give the title compound as a light brown powder (8.60 g, 80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08822503B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-747c719673c14319976281b8344aa4fe |
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| Source note | uspto-grants-2014_09 |
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