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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1970952Generated: November 3, 2026

Trimethylsilylacetylene → 3-Bromo-5-((trimethylsilyl)ethynyl)pyridine

https://huagongshe.com/reaction/1970952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant3,5-DibromopyridineHCID 69369—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
Product3-Bromo-5-((trimethylsilyl)ethynyl)pyridineHCID 66524424—

Reaction Steps

To a solution of 3,5-dibromopyridine (1.0 eq, 5.0 g, 20.9 mmol) in TEA (100 ml) under an inert atmosphere of nitrogen is added copper(I) iodide (0.1 eq, 406 mg, 2.09 mmol) and PdCl2(PPh3)2 (0.1 eq, 1.5 g, 2.09 mmol). Trimethylsilylacetylene (1.2 eq, 3.6 ml, 25 mmol) is added and the resulting mixture is stirred at room temperature for 2 h. The solvent is removed in vacuo and the residue is partitioned between water and DCM. The organic portion is separated and washed with sat. aqueous NaHCO3 solution, dried (MgSO4) and concentrated in vacuo. Purification by column chromatography (hexane/DCM) yields the title compound; [M+H]+=254/256.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431578B2
Source datasetuspto-grants-2013_04
ORD IDord-2ea010415cea409891e197c183c89677
Source noteuspto-grants-2013_04