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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17104Generated: October 25, 2026

Triethylamine → 3-Fluoro-5-((trimethylsilyl)ethynyl)benzonitrile

https://huagongshe.com/reaction/17104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant3-Bromo-5-fluorobenzonitrileHCID 2783330—
SolventTolueneHCID 1140—
Product3-Fluoro-5-((trimethylsilyl)ethynyl)benzonitrileHCID 16737211—

Reaction Conditions

Temperature95 °C

Reaction Steps

A solution of 3-bromo-5-fluorobenzonitrile (2.5 g, 12.5 mmol), (trimethylsilyl)acetylene (2.86 ml, 20 mmol), bis(acetate)bis(triphenylphoshpino) Palladium(II) (936 mg, 1.25 mmol) and triethylamine (35 ml) in toluene (35 ml) was 15 degassed by bubbling nitrogen through the solution and then stirred at 95° C. for 30 minutes. Filtration and concentration to yield a crude product. It was diluted with EtOAc (150 ml). The organic phase was washed with saturated NaHCO3 solution (50 ml), brine (50 ml) and the organic layer was dried over sodium sulfate. Filtration and concentration to yield a product A293.1 (2.4 g, 88%). HPLC: 95%, retention time: 4.05 minute (condition A). LC/MS (M+H)+=218.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737279B2
Source datasetuspto-grants-2010_06
ORD IDord-bd280274d3164bc1abeaa913cf194cbf
Source noteuspto-grants-2010_06