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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340286Generated: October 30, 2026

Triethylamine → Ethyl 3-methyl-4-((triethylsilyl)ethynyl)benzoate

https://huagongshe.com/reaction/340286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant(Triethylsilyl)acetyleneHCID 637947—
ReactantEthyl 4-bromo-3-methylbenzoateHCID 21729626—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
SolventAmmonium HydroxideHCID 14923—
ProductEthyl 3-methyl-4-((triethylsilyl)ethynyl)benzoateHCID 66874679—

Reaction Steps

A solution of ethyl 4-bromo-3-methylbenzoate (from the previous step) (1.0 eq.), triethyl(ethynyl)silane (1.1 eq.), trans-dichlororbis(triphenylphosphine)palladium (II) (10 mol %), copper (I) iodide (20 mol %), and triethylamine (5.0 eq.) in DMF (0.3 M) was stirred at 60° C. overnight. After cooling to ambient temperature, the reaction mixture was diluted with ethyl acetate and 10% aqueous ammonium hydroxide. The two phases were separated, and the aqueous layer was extracted twice with ethyl acetate. The combined organic layers were washed with brine, dried over anhydrous MgSO4, and concentrated en vacuo. The crude material was purified by flash chromatography on a COMBIFLASH® system (ISCO) using 0-5% ethyl acetate in hexane to give ethyl 3-methyl-4-((triethylsilyl)ethynyl)benzoate as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895577B2
Source datasetuspto-grants-2014_11
ORD IDord-e7d1da00bdf544eb8d3d21076df84a62
Source noteuspto-grants-2014_11