(Z)-N-(4-acetylphenyl)-2-(4-((2,4-dioxothiazolidin-5-ylidene)methyl)phenoxy)acetamide

Base Information

Chemical Name:(Z)-N-(4-acetylphenyl)-2-(4-((2,4-dioxothiazolidin-5-ylidene)methyl)phenoxy)acetamide
CAS No.:1266715-46-1
Molecular Formula:C₂₀H₁₆N₂O₅S
Molecular Weight:396.423
Hs Code.:

Synonyms:(Z)-N-(4-acetylphenyl)-2-(4-((2,4-dioxothiazolidin-5-ylidene)methyl)phenoxy)acetamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (Z)-N-(4-acetylphenyl)-2-(4-((2,4-dioxothiazolidin-5-ylidene)methyl)phenoxy)acetamide

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Technology Process of (Z)-N-(4-acetylphenyl)-2-(4-((2,4-dioxothiazolidin-5-ylidene)methyl)phenoxy)acetamide

There total 3 articles about (Z)-N-(4-acetylphenyl)-2-(4-((2,4-dioxothiazolidin-5-ylidene)methyl)phenoxy)acetamide 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: 84.0%

: 2295-31-0
thiazoline-2,4-dione

: 331962-59-5
N-(4-acetylphenyl)-2-(4-formylphenoxy)acetamide

: 1266715-46-1
(Z)-N-(4-acetylphenyl)-2-(4-((2,4-dioxothiazolidin-5-ylidene)methyl)phenoxy)acetamide

Guidance literature:: With acetic acid; 3-amino propanoic acid; for 4h; Reflux;
DOI:10.1021/jm1011534

Reference yield:

: 38283-38-4
4-(2-chloroacetamido)acetophenone

: 1266715-46-1
(Z)-N-(4-acetylphenyl)-2-(4-((2,4-dioxothiazolidin-5-ylidene)methyl)phenoxy)acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate; potassium iodide / acetone / 24 h / Reflux

2: acetic acid; 3-amino propanoic acid / 4 h / Reflux

With potassium carbonate; acetic acid; potassium iodide; 3-amino propanoic acid; In acetone; 2: Knoevenagel reaction;
DOI:10.1021/jm1011534

Reference yield:

: 99-92-3
p-aminobenzophenone

: 1266715-46-1
(Z)-N-(4-acetylphenyl)-2-(4-((2,4-dioxothiazolidin-5-ylidene)methyl)phenoxy)acetamide

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / dichloromethane / 0 - 25 °C

2: potassium carbonate; potassium iodide / acetone / 24 h / Reflux

3: acetic acid; 3-amino propanoic acid / 4 h / Reflux

With potassium carbonate; acetic acid; triethylamine; potassium iodide; 3-amino propanoic acid; In dichloromethane; acetone; 3: Knoevenagel reaction;
DOI:10.1021/jm1011534