(Z)-5-(4-(2-(2-chlorophenyl)-2-oxoethoxy)benzylidene)-2-thioxothiazolidin-4-one

Base Information

Chemical Name:(Z)-5-(4-(2-(2-chlorophenyl)-2-oxoethoxy)benzylidene)-2-thioxothiazolidin-4-one
CAS No.:1393890-89-5
Molecular Formula:C₁₈H₁₂ClNO₃S₂
Molecular Weight:389.883
Hs Code.:

Synonyms:(Z)-5-(4-(2-(2-chlorophenyl)-2-oxoethoxy)benzylidene)-2-thioxothiazolidin-4-one

Suppliers and Price of (Z)-5-(4-(2-(2-chlorophenyl)-2-oxoethoxy)benzylidene)-2-thioxothiazolidin-4-one

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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)-5-(4-(2-(2-chlorophenyl)-2-oxoethoxy)benzylidene)-2-thioxothiazolidin-4-one

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Technology Process of (Z)-5-(4-(2-(2-chlorophenyl)-2-oxoethoxy)benzylidene)-2-thioxothiazolidin-4-one

There total 3 articles about (Z)-5-(4-(2-(2-chlorophenyl)-2-oxoethoxy)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: 87.0%

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

: 1393890-84-0
C₁₅H₁₁ClO₃

: 1393890-89-5
(Z)-5-(4-(2-(2-chlorophenyl)-2-oxoethoxy)benzylidene)-2-thioxothiazolidin-4-one

Guidance literature:: With piperidine; acetic acid; In ethanol; for 4h; Reflux;
DOI:10.1016/j.ejmech.2012.05.023

Reference yield:

: 5000-66-8
2-chlorophenacyl bromide

: 1393890-89-5
(Z)-5-(4-(2-(2-chlorophenyl)-2-oxoethoxy)benzylidene)-2-thioxothiazolidin-4-one

Guidance literature:: Multi-step reaction with 2 steps

1: acetone / 20 °C

2: piperidine; acetic acid / ethanol / 4 h / Reflux

With piperidine; acetic acid; In ethanol; acetone; 2: Knoevenagel condensation;
DOI:10.1016/j.ejmech.2012.05.023

Reference yield:

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

: 1393890-89-5
(Z)-5-(4-(2-(2-chlorophenyl)-2-oxoethoxy)benzylidene)-2-thioxothiazolidin-4-one

Guidance literature:: Multi-step reaction with 3 steps

1: toluene-4-sulfonic acid; N,N'-dibromohydantoin / methanol / 8 h / 30 °C

2: acetone / 20 °C

3: piperidine; acetic acid / ethanol / 4 h / Reflux

With piperidine; toluene-4-sulfonic acid; acetic acid; N,N'-dibromohydantoin; In methanol; ethanol; acetone; 3: Knoevenagel condensation;
DOI:10.1016/j.ejmech.2012.05.023