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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042851Generated: November 1, 2026

2-Bromo-3-pyridinol → 2-(Trimethylsilyl)furo[3,2-b]pyridine

https://huagongshe.com/reaction/1042851

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-3-pyridinolHCID 23070—
ReactantTrimethylsilylacetyleneHCID 66111—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
Solvent1,4-DioxaneHCID 31275—
Product2-(Trimethylsilyl)furo[3,2-b]pyridineHCID 13636539—

Reaction Conditions

Temperature50 °C

Reaction Steps

A sealed pressure flask was charged with 2-bromopyridin-3-ol (10.0 g, 57.5 mmol), ethynyltrimethylsilane (15.9 ml, 115 mmol), copper (I) iodide (1.09 g, 5.75 mmol), bis(triphenylphosphine)palladium(II) chloride (2.02 g, 2.87 mmol) and 7.5 mL of dioxane. Ethynyltrimethylsilane (15.9 ml, 115 mmol) and TEA (40.0 ml, 287 mmol) were added, the vial was flushed with nitrogen, and the reaction was stirred at 50° C. for 18 h. The reaction was concentrated and purified via column chromatography (gradient elution 0-40% EtOAc:Hex) to afford 2-(trimethylsilyl)furo[3,2-b]pyridine as a brown oil. MS Found M+H+=192.3

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557816B2
Source datasetuspto-grants-2013_10
ORD IDord-4d675f4eb839421f9d166500cd977a3b
Source noteuspto-grants-2013_10