(E)-5-(4-((E)-3-(2-chlorophenyl)-3-oxoprop-1-enyl)benzylidene)-2-thioxothiazolidin-4-one

Base Information

Chemical Name:(E)-5-(4-((E)-3-(2-chlorophenyl)-3-oxoprop-1-enyl)benzylidene)-2-thioxothiazolidin-4-one
CAS No.:1414806-90-8
Molecular Formula:C₁₉H₁₂ClNO₂S₂
Molecular Weight:385.895
Hs Code.:

Synonyms:(E)-5-(4-((E)-3-(2-chlorophenyl)-3-oxoprop-1-enyl)benzylidene)-2-thioxothiazolidin-4-one

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Chemical Property of (E)-5-(4-((E)-3-(2-chlorophenyl)-3-oxoprop-1-enyl)benzylidene)-2-thioxothiazolidin-4-one

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Technology Process of (E)-5-(4-((E)-3-(2-chlorophenyl)-3-oxoprop-1-enyl)benzylidene)-2-thioxothiazolidin-4-one

There total 3 articles about (E)-5-(4-((E)-3-(2-chlorophenyl)-3-oxoprop-1-enyl)benzylidene)-2-thioxothiazolidin-4-one 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: 36.0%

: 141-84-4
2-thioxo-4-thiazolidinone

: 1261352-77-5
C₁₆H₁₁ClO₂

: 1414806-90-8
(E)-5-(4-((E)-3-(2-chlorophenyl)-3-oxoprop-1-enyl)benzylidene)-2-thioxothiazolidin-4-one

Guidance literature:: With piperidine; acetic acid; In ethanol; for 12h; Reflux;
DOI:10.1016/j.ejmech.2012.08.026

Reference yield:

: 2142-68-9
1-(2-chlorophenyl)ethanone

: 1414806-90-8
(E)-5-(4-((E)-3-(2-chlorophenyl)-3-oxoprop-1-enyl)benzylidene)-2-thioxothiazolidin-4-one

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydroxide / ethanol / 23 °C

2: piperidine; acetic acid / ethanol / 12 h / Reflux

With piperidine; acetic acid; sodium hydroxide; In ethanol; 1: |Claisen-Schmidt Condensation;
DOI:10.1016/j.ejmech.2012.08.026

Reference yield:

: 623-27-8
terephthalaldehyde,

: 1414806-90-8
(E)-5-(4-((E)-3-(2-chlorophenyl)-3-oxoprop-1-enyl)benzylidene)-2-thioxothiazolidin-4-one

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydroxide / ethanol / 23 °C

2: piperidine; acetic acid / ethanol / 12 h / Reflux

With piperidine; acetic acid; sodium hydroxide; In ethanol; 1: |Claisen-Schmidt Condensation;
DOI:10.1016/j.ejmech.2012.08.026