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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387717Generated: November 1, 2026

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

https://huagongshe.com/reaction/2387717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant3-Bromo-5-fluorobenzonitrileHCID 2783330—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventTetrahydrofuranHCID 8028—
Product3-Fluoro-5-((trimethylsilyl)ethynyl)benzonitrileHCID 16737211—

Reaction Steps

To a solution of commercially available 3-bromo-5-fluorobenzonitrile (5 g, 25 mmol) and triethylamine (35 ml) in 35 ml of THF was bubbled nitrogen for 10 min. Then added trimethylsilylacetylene (5.0 g, 50 mmol), copper iodide (60 mg, 0.31 mmol), and PdCl2(PPh3)2 (80 mg, 0.11 mmol) and the reaction mixture was heated with a heating mantle. After an initial exotherm, the reaction was heated at reflux for 3 hrs. The reaction mixture was concentrated on a rotary evaporator and the dark residue diluted with hexane and washed with water three times. The hexane layer was filtered through Celite and the filtrate was concentrated to give a brown oil. The crude material was used without further purification. LCMS B: Ret time 3.96 min, (M+H)+=218.14. 1H NMR, 400 MHz, CDCl3: 7.57 (s, 1H), 7.43 (m, 1H), 7.35 (m, 1H), 0.26 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268855B2
Source datasetuspto-grants-2012_09
ORD IDord-5ec3ced2816344ee85e869c7732e2cb5
Source noteuspto-grants-2012_09