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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPropargyl alcoholHCID 7859—
ReactantTriethylamineHCID 8471—
Reactant6-Bromo-3-chloro-2-methoxypyridineHCID 58452302—
CatalystCopper iodideHCID 83717—
SolventEthyl AcetateHCID 8857—
Product3-(5-Chloro-6-methoxypyridin-2-yl)prop-2-yn-1-olHCID 5845266780%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822503B2
Source datasetuspto-grants-2014_09
ORD IDord-747c719673c14319976281b8344aa4fe
Source noteuspto-grants-2014_09