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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561005Generated: October 31, 2026

Triethylamine → 4-Chloro-3-((trimethylsilyl)ethynyl)pyridine

https://huagongshe.com/reaction/561005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTriphenylphosphineHCID 11776—
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant4-Chloro-3-iodopyridineHCID 2763163—
CatalystCopper iodideHCID 83717—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
Product4-Chloro-3-((trimethylsilyl)ethynyl)pyridineHCID 4631815896.5%

Reaction Steps

To a solution of 4-chloro-3-iodo pyridine (2.0 g, 8.3 mmol) in toluene (20 mL) add triphenyl phosphine (0.219 g, 0.83 mmol), copper iodide (0.079 g, 0.41 mmol) and palladium (II) acetate (0.093 g, 0.41 mmol), add triethylamine (3.49 mL, 25 mmol) dropwise at room temperature followed by the addition of trimethylsilylacetylene (1.65 mL, 11.69 mmol) at room temperature with continuous stirring. Stir the reaction mixture at room temperature for 2 hours. Concentrate the reaction mixture by evaporating the toluene under vacuum. Extract the compound (almost pure) by triturating with hexane and then decanting the hexane layer 4 to 5 times. Evaporate hexane under vacuum and dry it to obtain the pure compound (1.68 g, 96%). 1H NMR (400 MHz, CDCl3) δ 8.677 (s, 1H), 8.418 (s, 1H), 7.338 (d, J=2.6 Hz, 1H), 0.286 (s, 9H). MS (ES) m/z 210 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063212B2
Source datasetuspto-grants-2011_11
ORD IDord-13b99fffe5614fe8a0fc023e5d67f019
Source noteuspto-grants-2011_11