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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479572Generated: November 4, 2026

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

https://huagongshe.com/reaction/1479572

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 vaccuo. 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 numberUS09408907B2
Source datasetuspto-grants-2016_08
ORD IDord-d9d67ede2559449ea13e8c06290e9a36
Source noteuspto-grants-2016_08