ethyl 4,5-dioxo-1-phenyl-2-(4-(4-(trifluoromethoxy)benzyl)phenyl)-4,5-dihydro-1H-pyrrole-3-carboxylate

Base Information

• Chemical Name: ethyl 4,5-dioxo-1-phenyl-2-(4-(4-(trifluoromethoxy)benzyl)phenyl)-4,5-dihydro-1H-pyrrole-3-carboxylate
• CAS No.: 1379615-53-8
• Molecular Formula: C₂₇H₂₀F₃NO₅
• Molecular Weight: 495.455
• Mol file: 1379615-53-8.mol

Synonyms:ethyl 4,5-dioxo-1-phenyl-2-(4-(4-(trifluoromethoxy)benzyl)phenyl)-4,5-dihydro-1H-pyrrole-3-carboxylate

Chemical Property of ethyl 4,5-dioxo-1-phenyl-2-(4-(4-(trifluoromethoxy)benzyl)phenyl)-4,5-dihydro-1H-pyrrole-3-carboxylate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of ethyl 4,5-dioxo-1-phenyl-2-(4-(4-(trifluoromethoxy)benzyl)phenyl)-4,5-dihydro-1H-pyrrole-3-carboxylate

There total 3 articles about ethyl 4,5-dioxo-1-phenyl-2-(4-(4-(trifluoromethoxy)benzyl)phenyl)-4,5-dihydro-1H-pyrrole-3-carboxylate 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: 45.0%

oxalyl dichloride (79-37-8) + (E)-ethyl 3-(phenylamino)-3-(4-(4-(trifluoromethoxy)benzyl)phenyl)acrylate (1361006-03-2) → ethyl 4,5-dioxo-1-phenyl-2-(4-(4-(trifluoromethoxy)benzyl)phenyl)-4,5-dihydro-1H-pyrrole-3-carboxylate (1379615-53-8)

Guidance literature:

In diethyl ether; at 5 - 50 ℃; for 2h;

Reference yield:

4-(4-(trifluoromethoxy)benzyl)benzaldehyde (1361005-59-5) → ethyl 4,5-dioxo-1-phenyl-2-(4-(4-(trifluoromethoxy)benzyl)phenyl)-4,5-dihydro-1H-pyrrole-3-carboxylate (1379615-53-8)

Guidance literature:

Multi-step reaction with 3 steps

1: niobium pentachloride / dichloromethane / 17 - 25 °C / Inert atmosphere

2: acetic acid / ethanol / Reflux

3: diethyl ether / 2 h / 5 - 50 °C

With acetic acid; niobium pentachloride; In diethyl ether; ethanol; dichloromethane;

Reference yield:

ethyl 3-oxo-3-(4-(4-(trifluoromethoxy)benzyl)phenyl)propanoate (1361005-34-6) → ethyl 4,5-dioxo-1-phenyl-2-(4-(4-(trifluoromethoxy)benzyl)phenyl)-4,5-dihydro-1H-pyrrole-3-carboxylate (1379615-53-8)

Guidance literature:

Multi-step reaction with 2 steps

1: acetic acid / ethanol / Reflux

2: diethyl ether / 2 h / 5 - 50 °C

With acetic acid; In diethyl ether; ethanol;

upstream raw materials:

oxalyl dichloride

(E)-ethyl 3-(phenylamino)-3-(4-(4-(trifluoromethoxy)benzyl)phenyl)acrylate

ethyl 3-oxo-3-(4-(4-(trifluoromethoxy)benzyl)phenyl)propanoate

4-(4-(trifluoromethoxy)benzyl)benzaldehyde

Downstream raw materials:

4-oxo-2-(4-(4-(trifluoromethoxy)benzyl)phenyl)-1,4-dihydroquinoline-3-carboxylic acid