(E)-2-(2-(5-(4-chlorophenyl)furan-2-yl)vinyl)-5-p-tolyl-1,3,4-oxadiazole

Base Information

Chemical Name:(E)-2-(2-(5-(4-chlorophenyl)furan-2-yl)vinyl)-5-p-tolyl-1,3,4-oxadiazole
CAS No.:1350920-06-7
Molecular Formula:C₂₁H₁₅ClN₂O₂
Molecular Weight:362.815
Hs Code.:

Synonyms:(E)-2-(2-(5-(4-chlorophenyl)furan-2-yl)vinyl)-5-p-tolyl-1,3,4-oxadiazole

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Chemical Property of (E)-2-(2-(5-(4-chlorophenyl)furan-2-yl)vinyl)-5-p-tolyl-1,3,4-oxadiazole

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Technology Process of (E)-2-(2-(5-(4-chlorophenyl)furan-2-yl)vinyl)-5-p-tolyl-1,3,4-oxadiazole

There total 2 articles about (E)-2-(2-(5-(4-chlorophenyl)furan-2-yl)vinyl)-5-p-tolyl-1,3,4-oxadiazole which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 71.0%

: 827-58-7
2-p-tolyl-1,3,4-oxadiazole

: 1350920-09-0
C₁₂H₈BrClO

: 1350920-06-7
(E)-2-(2-(5-(4-chlorophenyl)furan-2-yl)vinyl)-5-p-tolyl-1,3,4-oxadiazole

Guidance literature:: With copper(l) iodide; lithium tert-butoxide; N,N`-dimethylethylenediamine; In dimethyl sulfoxide; at 70 ℃; for 3h; Inert atmosphere;
DOI:10.1016/j.tet.2011.10.049

Reference yield:

: 62806-34-2,58110-37-5
(E)-3-[5-(4-chlorophenyl)-2-furyl]-2-propenoic acid

: 1350920-06-7
(E)-2-(2-(5-(4-chlorophenyl)furan-2-yl)vinyl)-5-p-tolyl-1,3,4-oxadiazole

Guidance literature:: Multi-step reaction with 2 steps

1.1: triethylamine / dichloromethane / 0.08 h / 20 °C

1.2: 0.17 h / 20 °C

2.1: copper(l) iodide; lithium tert-butoxide; N,N`-dimethylethylenediamine / dimethyl sulfoxide / 3 h / 70 °C / Inert atmosphere

With copper(l) iodide; triethylamine; lithium tert-butoxide; N,N`-dimethylethylenediamine; In dichloromethane; dimethyl sulfoxide;
DOI:10.1016/j.tet.2011.10.049