Réaction #792201

ord-bfc4bfa4da534542bf1ad45ec822b58e

Équation de réaction

C(=NNc1ccccc1)/C(=N\Nc1ccccc1)c1ccco1
(2E)-2,2′-(1-(furan-2-yl)ethane-1,2-diylidene)bis(1-phenylhydrazine)
c1ccc(-n2ncc(-c3ccco3)n2)cc1
4-(furan-2-yl)-2-phenyl-2H-1,2,3-triazole
Rendement 57.7%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurewhile heating
  2. 2
    Températureunder reflux
  3. 3
    workup.ADDITIONAfter complete addition
  4. 4
    Températureheating
  5. 5
    AutreThe solvent was then evaporated to dryness

Mode opératoire

An aqueous solution of hydrated copper sulphate (421 mg, 1.68 mmol) in 2 mL of demineralized water was added portion-wise to a solution of (2E)-2,2′-(1-(furan-2-yl)ethane-1,2-diylidene)bis(1-phenylhydrazine) (150 mg, 0.493 mmol) in dioxane (3.3 ml) while heating under reflux. After complete addition, heating was continued further for 2 hours. The solvent was then evaporated to dryness. The resulting crude material was subjected to flash column chromatography using an ethyl acetate/hexane solvent system (1-1.5%) to yield the desired compound 4-(furan-2-yl)-2-phenyl-2H-1,2,3-triazole as a yellow solid (60 mg, 57.7%). The HPLC purity of the final product was 96.03%. LC-MS [M+1] (C12H9N3O+H expected 212.07). The melting point of the final compound was observed to be 80° C. The 1H-NMR spectra was in accordance with the chemical structure.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09173401B2uspto-grants-2015_11