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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 76138Generated: October 29, 2026

Trimethylsilylacetylene → 2-(4-Methoxyphenyl)-5-((trimethylsilyl)ethynyl)pyrazine

https://huagongshe.com/reaction/76138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantHCID 87073288HCID 87073288—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Methoxyphenyl)-5-((trimethylsilyl)ethynyl)pyrazineHCID 66611167—

Reaction Steps

A mixture of 2.30 g (7.37 mmol) 2-iodo-5-(4-methoxyphenyl)pyrazine and 1.56 mL (11.1 mmol) ethynyltrimethylsilane in 30 mL THF is charged with 0.12 g (0.15 mmol) bis(triphenylphosphine)dichloropalladium, 0.03 g (15.0 mmol) CuI and 3.01 mL (22.1 mmol) TEA. After stirring at r.t. for 4 h the reaction mixture is diluted with DCM and washed with 50 mL aq. 5% ammonia solution (1×) and 50 mL water (1×). The organic layer is dried with MgSO4 and the solvent is removed in vacuo. The residue is treated with PE/EtOAc (8/2), filtered through a plug of silica gel and the solvent is again removed in vacuo. The product is used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835472B2
Source datasetuspto-grants-2014_09
ORD IDord-27a272c13c374066899505257c6b414e
Source noteuspto-grants-2014_09