HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1476682Generated: October 30, 2026
Pentamethyldiethylenetriamine → HCID 90410677, compound
https://huagongshe.com/reaction/1476682
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pentamethyldiethylenetriamine | HCID 18196 | — |
| Reactant | Azidobenzene | HCID 69319 | — |
| Reactant | 2-[(Trimethylsilyl)ethynyl]thiophene | HCID 596870 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 90410677 | HCID 90410677 | 47,533.301% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09402397B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-4c32fee4ccf84219a95c4ae2adb397f5 |
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| Source note | uspto-grants-2016_08 |
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