تفاعل #1563862

ord-1242d02907a944959b074b927006b1df

معادلة التفاعل

C[SiH](C)C
trimethylsilane
[N-]=[N+]=Nc1ccccc1
phenyl azide
CN(C)CCN(C)CCN(C)C
1,1,4,7,7-pentamethyldiethlene triamine
CCCC[N+](CCCC)(CCCC)CCCC.[F-]
TBAF
C1CCOC1
THF
c1ccc(-n2cc(-c3ccco3)nn2)cc1
4-(furan-2-yl)-1-phenyl-1H-1,2,3-triazole
المردود 62.2%

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 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.

المصدر

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