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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491305Generated: October 27, 2026

Triethylamine → HCID 178432714, compound

https://huagongshe.com/reaction/491305

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTriphenylphosphineHCID 11776—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant4-[2-(Trimethylsilyl)ethynyl]pyridine-2-carbonitrileHCID 45116446—
ReactantHCID 178433060HCID 178433060—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178432714HCID 178432714—

Reaction Conditions

Temperature60 °C

Reaction Steps

Triphenylphosphine (126 mg, 0.48 mmol), bis(triphenylphosphine)palladium (II) chloride (1.01 g, 1.44 mmol) and triethylamine (3.65 g, 101.2 mmol) were dissolved in 40 ml of dry THF. This mixture was evacuated and backfilled with argon several times to remove oxygen from the solution. 4-iodo-2-methyl-1H-imidazole [Tetrahedron Letters 30(11), 1409 (1989)] (5.0 g, 20.8 mmol), 4-trimethylsilanylethynyl-pyridine-2-carbonitrile (4.43 g, 22.1 nmol) and copper (1) iodide (46 mg, 0.24 mmol) were added and the mixture was warmed to 60° C. A 1M solution of tetrabutylammonium fluoride (24 ml, 24.0 mmol) was added dropwise over a period of 30 min. After the addition was finished, the reaction mixture was stirred at 60° C. for another hour. The solvent was evaporated. The residue was taken up in 200 mL water and extracted three times with 200 ml of ethyl acetate. The combined organic extracts were dried with magnesium sulfate, filtered and evaporated. The crude product was purified by flash chromatography on silica gel (methanol/methylene chloride 5:95). The desired product was obtained as a light yellow solid (1.06 g, 21%). MS: m/e=208.9 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531529B2
Source datasetuspto-grants-2009_05
ORD IDord-f3e336aa5afa4a6881720bfeea2d9a34
Source noteuspto-grants-2009_05