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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2244336Generated: November 2, 2026

Trimethylsilylacetylene → 2-Chloro-4-(2-(trimethylsilyl)ethynyl)pyridine

https://huagongshe.com/reaction/2244336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant4-Bromo-2-chloropyridineHCID 3847770—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventTriethylamineHCID 8471—
Product2-Chloro-4-(2-(trimethylsilyl)ethynyl)pyridineHCID 2198539191%

Reaction Steps

A mixture of 2.5 g of 4-bromo-2-chloropyridine (12.6 mmol), 2.2 ml of (trimethylsilyl)acetylene (15.1 mmol), 153 mg of copper(I)iodide (0.79 mmol) and 287 mg of bis(triphenylphosphine)palladium(II)chloride (0.41 mmol) in triethylamine (15 ml) was stirred at RT for 1 h. The triethylamine was then removed in vacuo, water was added and the mixture was extracted with diethylether. The combined organic extracts were then washed with water and brine, dried (Na2SO4), filtered and concentrated in vacuo to give a residue which was purified by column chromatography (heptane/EtOAc 100:0 to 98:2) to give 2-chloro-4-trimethylsilanylethynyl-pyridine (2.394 g, 91%) as a light yellow liquid. MS (ISP) 210.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07678818B2
Source datasetuspto-grants-2010_03
ORD IDord-1d1f81230e4c484fbf9a5652da30950b
Source noteuspto-grants-2010_03