Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416540Generated: November 1, 2026

Propargyl alcohol → 3-(3-(Pyridin-2-yl)isoxazol-5-yl)prop-2-yn-1-ol

https://huagongshe.com/reaction/2416540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl alcoholHCID 7859—
Reactant2-(5-Iodo-3-isoxazolyl)pyridineHCID 11149943—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
Product3-(3-(Pyridin-2-yl)isoxazol-5-yl)prop-2-yn-1-olHCID 2263082122%

Reaction Conditions

Temperature65 °C

Reaction Steps

A solution of 2-(5-iodo-3-isoxazolyl)pyridine (prepared as described in WO0232919, 1.38 g, 5 mmol) and dichlorobis(triphenylphosphine)palladium(II) (35 mg, 0.05 mmol) in 8 mL triethylamine was degassed with nitrogen. Propargyl alcohol (560 mg, 10 mmol) was added and the mixture was heated at 65° C. for 16 h. The reaction mixture was cooled to room temperature, concentrated to remove the solvent. The residue was diluted with ethyl acetate (100 mL), washed with saturated NaHCO3, water and brine. The organic layer was dried and concentrated. Purification by chromatography (SiO2, 1:1 hexane/ethyl acetate) yielded 220 mg (22%) of the title compound. MS 201 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06825170B2
Source datasetuspto-grants-2004_11
ORD IDord-91ad6aa925084cb794ab447d20a021fb
Source noteuspto-grants-2004_11