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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1476682Generated: October 30, 2026

Pentamethyldiethylenetriamine → HCID 90410677, compound

https://huagongshe.com/reaction/1476682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPentamethyldiethylenetriamineHCID 18196—
ReactantAzidobenzeneHCID 69319—
Reactant2-[(Trimethylsilyl)ethynyl]thiopheneHCID 596870—
ReactantTetrabutylammonium FluorideHCID 2724141—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTetrahydrofuranHCID 8028—
ProductHCID 90410677HCID 9041067747,533.301%

Reaction Steps

To a solution of trimethyl(thiophen-2-ylethynyl)silane (50 mg, 0.2777 mmol), phenyl azide (0.5 M solution, 1.1 ml, 0.555 mmol), and CuI (52.87 mg, 0.2777 mmol) in THF (1 ml) was added 1,1,4,7,7-pentamethyldiethlenetriamine (0.116 ml, 0.555 mmol) and 1M TBAF.3H2O (0.554 ml, 0.554 mmol). After stirring the reaction mixture for 20 hours at room temperature, it was quenched with saturated ammonium chloride solution and was extracted with ethyl acetate. The combined organic layers were washed with water, dried over anhydrous sodium sulfate and evaporated. The crude material was purified by column chromatography (100-200 mesh silica gel) using 5% ethyl acetate in hexane as eluant to yield 1-phenyl-4-(thiophen-2-yl)-1H-1,2,3-triazole (30 mg, 0.132 mol, yield 47.61%) with an HPLC purity of 97.64%. LC-MS [M+H] 228.2 (C12H9N3S+H, expected 228.05). The 1H-NMR spectra was in accordance with the chemical structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09402397B2
Source datasetuspto-grants-2016_08
ORD IDord-4c32fee4ccf84219a95c4ae2adb397f5
Source noteuspto-grants-2016_08