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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654963Generated: October 30, 2026

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

https://huagongshe.com/reaction/654963

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopyridineHCID 7973—
ReactantTriphenylphosphineHCID 11776—
ReactantSodium HydroxideHCID 14798—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Catalystpalladium(II) acetateHCID 167845—
SolventTriethylamineHCID 8471—
Product3-(Pyridin-2-yl)prop-2-yn-1-olHCID 3481147—

Reaction Steps

A mixture of 2-bromopyridine (5 g, 31.6 mmol), palladium (II) acetate (5 mg), copper (I) iodide (5 mg), triphenylphosphine (5 mg) in triethylamine (50 ml) was deaerated with argon for 5 minutes. After propagyl alcohol (2.2 ml, 38.0 mmol) was added, the solution was rapidly heated to reflux under argon and conditions maintained for 17 h. On cooling, the mixture was poured into 2M sodium hydroxide (ca. 30 ml) and extracted thoroughly with ethyl acetate. Evaporation of the dried (magnesium sulphate) extracts gave an oil, which was flash chromatographed on silica using 80% ethyl acetate/chloroform. Fractions with Rf of about 0.23 on evaporation gave the title alcohol as a light tan solid: mp 78°-80°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05134128
Source datasetuspto-grants-1992_07
ORD IDord-919e0253faf74e2e91942a7c466055f4
Source noteuspto-grants-1992_07