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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2375752Generated: October 29, 2026

Triethylamine → 4-Amino-5-ethynyl-2-(trifluoromethyl)benzenecarbonitrile

https://huagongshe.com/reaction/2375752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant4-Amino-5-iodo-2-(trifluoromethyl)benzonitrileHCID 25067377—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTetrahydrofuranHCID 8028—
Product4-Amino-5-ethynyl-2-(trifluoromethyl)benzenecarbonitrileHCID 66545172—

Reaction Steps

4-Amino-5-iodo-2-trifluoromethyl-benzonitrile (936 mg, 3.0 mmol), CuI (I) (57 mg, 0.3 mmol), PdCl2(PPh3)2 (105.3 mg, 0.15 mmol), triethylamine (1.01 g, 10 mmol) and ethynyl-trimethyl-silane (450 mg, 4.5 mmol) were mixed in THF (30 ml). The reaction mixture was stirred at room temperature overnight. Tetrabutylammonium fluoride (1.0 M in THF, 3.0 ml, 3.0 mmol) was added to the reaction mixture, which was then stirred at room temperature for 20 mins. The reaction mixture was quenched by addition of H2O and extracted with ethyl acetate. The organic layers were combined and washed with brine, dried over Na2SO4 and concentrated to yield crude product 4-amino-5-ethynyl-2-trifluoromethyl-benzonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07465809B2
Source datasetuspto-grants-2008_12
ORD IDord-bb58a19b295b46fab7c49a680e528f57
Source noteuspto-grants-2008_12