3-acetyl-5-(4-nitrophenyl)-2-(5-nitrothiophen-2-yl)-2,3-dihydro-1,3,4-oxadiazole

Base Information

• Chemical Name: 3-acetyl-5-(4-nitrophenyl)-2-(5-nitrothiophen-2-yl)-2,3-dihydro-1,3,4-oxadiazole
• CAS No.: 1345861-05-3
• Molecular Formula: C₁₄H₁₀N₄O₆S
• Molecular Weight: 362.323
• Mol file: 1345861-05-3.mol

Synonyms:3-acetyl-5-(4-nitrophenyl)-2-(5-nitrothiophen-2-yl)-2,3-dihydro-1,3,4-oxadiazole

Chemical Property of 3-acetyl-5-(4-nitrophenyl)-2-(5-nitrothiophen-2-yl)-2,3-dihydro-1,3,4-oxadiazole

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 3-acetyl-5-(4-nitrophenyl)-2-(5-nitrothiophen-2-yl)-2,3-dihydro-1,3,4-oxadiazole

There total 4 articles about 3-acetyl-5-(4-nitrophenyl)-2-(5-nitrothiophen-2-yl)-2,3-dihydro-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: 57.0%

4-nitrobenzoic acid [((5-nitro)thiophen-2-yl)methylene]hydrazide + acetic anhydride (108-24-7) → 3-acetyl-5-(4-nitrophenyl)-2-(5-nitrothiophen-2-yl)-2,3-dihydro-1,3,4-oxadiazole (1345861-05-3)

Guidance literature:

at 85 - 120 ℃; for 8h;

DOI:10.1016/j.bmc.2011.09.009

Reference yield:

4-nitrobenzoic acid methyl ester (619-50-1) → 3-acetyl-5-(4-nitrophenyl)-2-(5-nitrothiophen-2-yl)-2,3-dihydro-1,3,4-oxadiazole (1345861-05-3)

Guidance literature:

Multi-step reaction with 3 steps

1: hydrazine hydrate / water / 0.17 h / 75 °C

2: sulfuric acid; acetic acid / methanol; water / 1 h / Reflux

3: 8 h / 85 - 120 °C

With sulfuric acid; hydrazine hydrate; acetic acid; In methanol; water;

DOI:10.1016/j.bmc.2011.09.009

Reference yield:

4-nitro-benzoic acid (62-23-7) → 3-acetyl-5-(4-nitrophenyl)-2-(5-nitrothiophen-2-yl)-2,3-dihydro-1,3,4-oxadiazole (1345861-05-3)

Guidance literature:

Multi-step reaction with 4 steps

1: sulfuric acid / 4 h / Reflux

2: hydrazine hydrate / water / 0.17 h / 75 °C

3: sulfuric acid; acetic acid / methanol; water / 1 h / Reflux

4: 8 h / 85 - 120 °C

With sulfuric acid; hydrazine hydrate; acetic acid; In methanol; water;

DOI:10.1016/j.bmc.2011.09.009

upstream raw materials:

acetic anhydride

5-nitro-2-thiophenecarboxaldehyde

N-amino-(4-nitrophenyl)carboxamide

4-nitrobenzoic acid methyl ester