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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51162Generated: October 28, 2026

Trimethylsilylacetylene → 2-Trimethylsilylethen-1-yl-benzoate

https://huagongshe.com/reaction/51162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantEthyl 4-iodobenzoateHCID 142891—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
Product2-Trimethylsilylethen-1-yl-benzoateHCID 85176850116.9%

Reaction Steps

A solution of ethyl 4-iodo-benzoate (55.2 g, 0.2 mol) in triethylamine (800 mL) was purged with argon. Copper iodide (1.1 g) and bis(triphenylphosphine)palladium(II) dichloride (7.0 g) were then added and the mixture was purged again. Trimethylsilylacetylene (42 mL, 0.3 mol) was then added at 0° C. for 30 minutes and the resulting mixture stirred at room temperature for 1 hour. The mixture was concentrated, triturated in hexane and filtered. The filtrate was concentrated to give ethyl 4-(2-trimethylsilylethen-1-yl-benzoate (51.5 g, 100% crude) as a black oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713515B2
Source datasetuspto-grants-2004_03
ORD IDord-a92f395686f04eabad4807d04060acee
Source noteuspto-grants-2004_03