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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013711Generated: November 1, 2026

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

https://huagongshe.com/reaction/1013711

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 numberUS07981891B2
Source datasetuspto-grants-2011_07
ORD IDord-8094ac24fd944ee1b12092ababb6d9e8
Source noteuspto-grants-2011_07