Реакция #1563864
ord-4c32fee4ccf84219a95c4ae2adb397f5
Уравнение реакции
Реактанты
Реагенты
Растворители
Условия реакции
Обработка
- 1Другоеit was quenched with saturated ammonium chloride solution
- 2Экстракцияwas extracted with ethyl acetate
- 3ПромывкаThe combined organic layers were washed with water
- 4Сушкаdried over anhydrous sodium sulfate
- 5Другоеevaporated
- 6ДругоеThe crude material was purified by column chromatography (100-200 mesh silica gel)
Методика
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.