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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1476680Generated: October 30, 2026

Tetrahydrofuran → HCID 86303505, compound

https://huagongshe.com/reaction/1476680

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantPentamethyldiethylenetriamineHCID 18196—
ReactantAzidobenzeneHCID 69319—
ReactantTrimethylsilaneHCID 70435—
ReactantTetrabutylammonium FluorideHCID 2724141—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
ProductHCID 86303505HCID 8630350562.18%

Reaction Steps

To a solution of furan-2-ylethynyl)trimethylsilane (100 mg, 0.6097 mmol), phenyl azide (0.5 M solution, 2.42 ml, 1.2195 mmol), and CuI (116.11 mg, 0.6097 mmol) in THF (2 ml) was added 1,1,4,7,7-pentamethyldiethlene triamine (0.254 ml, 1.2195 mmol) and 1M TBAF.3H2O (1.20 ml, 1.2195 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 eluent to yield 4-(furan-2-yl)-1-phenyl-1H-1,2,3-triazole (80 mg, 0.378 mmol, yield 62.18%) with an HPLC purity of 98.82%. LC-MS [M+H] 212 (C12H9N3O+H expected 212.07), mp 118-120° C. 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-1242d02907a944959b074b927006b1df
Source noteuspto-grants-2016_08