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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17114Generated: October 30, 2026

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

https://huagongshe.com/reaction/17114

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 numberUS07737279B2
Source datasetuspto-grants-2010_06
ORD IDord-474f864f889d4824bbd1da6e2eef21b2
Source noteuspto-grants-2010_06