Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503586Generated: October 30, 2026

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

https://huagongshe.com/reaction/503586

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 numberUS07776857B2
Source datasetuspto-grants-2010_08
ORD IDord-7980de27edaf44a0a2643814285dd86f
Source noteuspto-grants-2010_08