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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709046Generated: October 25, 2026

Trimethylsilylacetylene → 2,3-Dimethoxy-5-[2-(trimethylsilyl)ethynyl]pyridine

https://huagongshe.com/reaction/709046

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant5-Bromo-2,3-dimethoxypyridineHCID 12563084—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
Product2,3-Dimethoxy-5-[2-(trimethylsilyl)ethynyl]pyridineHCID 4673783871%

Reaction Steps

Copper (I) iodide (0.56 g, 2.9 mmol), bis(triphenylphosphine)palladium(II) dichloride (2.1 g, 2.9 mmol), and 5-bromo-2,3-dimethoxypyridine (12.8 g, 59 mmol) were added to triethylamine (80 ml) which produced a yellow suspension. The reaction was thoroughly degassed and ethynyltrimethylsilane (5.8 g, 59 mmol) was added to the stirred suspension which was then stirred for 16 hours and concentrated. The crude material was purified by column chromatography (SiO2; 0-10% ethyl acetate in petrol) to afford 2,3-dimethoxy-5-[(trimethylsilyl)ethynyl]pyridine (9.8 g, 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09180122B2
Source datasetuspto-grants-2015_11
ORD IDord-d057327a4502493bb3831f6eb56adfea
Source noteuspto-grants-2015_11