反応 #1563864

反応方程式

trimethyl(thiophen-2-ylethynyl)silane

phenyl azide

1,1,4,7,7-pentamethyldiethlenetriamine

TBAF

→

1-phenyl-4-(thiophen-2-yl)-1H-1,2,3-triazole

溶媒

THF

反応条件

後処理

1. 1
   その他it was quenched with saturated ammonium chloride solution
2. 2
   抽出was extracted with ethyl acetate
3. 3
   洗浄The combined organic layers were washed with water
4. 4
   乾燥dried over anhydrous sodium sulfate
5. 5
   その他evaporated
6. 6
   その他The crude material was purified by column chromatography (100-200 mesh silica gel)

実験手順

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.

出典