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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334546Generated: October 26, 2026

2-Bromopyridine → 4-(Pyridin-2-yl)but-3-yn-1-ol

https://huagongshe.com/reaction/334546

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopyridineHCID 7973—
Reactant3-Butyn-1-OLHCID 13566—
CatalystCID 44148441HCID 44148441—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
Product4-(Pyridin-2-yl)but-3-yn-1-olHCID 1100806374.7%

Reaction Steps

In a dry reaction tube containing in suspension iodide copper (38 mg, 0.2 mmol) and triethylamine (11 mL, 80 mmol), were added 2-bromopyridine (632 mg, 4 mmol) and Pd(PPh3)2Cl2 (140 mg, 0.2 mmol). A yellow suspension is obtained and after a few minutes of stirring at room temperature, was added a solution of but-3-yn-1-ol (280 mg, 4 mmol) in triethylamine (2.2 mL). Immediately the color of the reaction turns to black. The mixture was stirred at room temperature for 30 min and then at 80° C. for 20 h. Triethylamine was concentrated under reduced pressure and the residue was dissolved in DCM. The organic layer was washed with saturated NH4Cl, water and brine, dried (MgSO4) and concentrated. The product was purified by flash chromatography (prepacked 15 g silicagel column, from DCM 100% to DCM/MeOH: 98/2 as eluent) to afford 440 mg of 4-(pyridin-2-yl)but-3-yn-1-ol (Yield: 74%) as brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883826B2
Source datasetuspto-grants-2014_11
ORD IDord-4a9667b8fb0d47a98cbc1518e0c63a26
Source noteuspto-grants-2014_11