تفاعل #1563864

ord-4c32fee4ccf84219a95c4ae2adb397f5

معادلة التفاعل

C[Si](C)(C)C#Cc1cccs1
trimethyl(thiophen-2-ylethynyl)silane
[N-]=[N+]=Nc1ccccc1
phenyl azide
CN(C)CCN(C)CCN(C)C
1,1,4,7,7-pentamethyldiethlenetriamine
CCCC[N+](CCCC)(CCCC)CCCC.[F-]
TBAF
c1ccc(-n2cc(-c3cccs3)nn2)cc1
1-phenyl-4-(thiophen-2-yl)-1H-1,2,3-triazole

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىit was quenched with saturated ammonium chloride solution
  2. 2
    استخلاصwas extracted with ethyl acetate
  3. 3
    غسيلThe combined organic layers were washed with water
  4. 4
    تجفيفdried over anhydrous sodium sulfate
  5. 5
    أخرىevaporated
  6. 6
    أخرىThe crude material was purified by column chromatography (100-200 mesh silica gel)

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09402397B2uspto-grants-2016_08