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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1463905Generated: November 2, 2026

Hydrochloric Acid → 3-(Pyridin-2-yl)prop-2-yn-1-ol

https://huagongshe.com/reaction/1463905

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPropargyl alcoholHCID 7859—
Reactant2-BromopyridineHCID 7973—
ReactantTriethylamineHCID 8471—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product3-(Pyridin-2-yl)prop-2-yn-1-olHCID 348114770%

Reaction Steps

2-Propynyl alcohol (35 ml) was added dropwise to a stirred mixture of 2-bromopyridine (23.7 g), bis(triphenylphosphine)palladium chloride (1.54 g), triethylamine (21 ml), cuprous iodide (1.5 g) and acetonitrile (150 ml) and the mixture was stirred at ambient temperature for 30 minutes and then heated to 60° C. for 2 hours. The mixture was cooled to ambient temperature, poured into water (200 ml) and neutralised by adding dilute aqueous hydrochloric acid. The mixture was extracted with methylene chloride (2×500 ml) and the combined extracts were washed with water (500 ml), dried (MgSO4) and evaporated. The residue was purified by column chromatography eluting with a 1:1 v/v mixture of methylene chloride and ethyl acetate to give 3-(2-pyridyl)prop-2-yn-1-yl alcohol (14 g, 70%), m.p. 78°-80° C. (recrystallised from a mixture of hexane and ethyl acetate).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05302603
Source datasetuspto-grants-1994_04
ORD IDord-d990328ae9f44b41848b3f13f54ea1d4
Source noteuspto-grants-1994_04