(S,Z)-2-(5-(4-(2-(2,4-dichlorophenyl)-2-oxoethoxy)benzylidene)-4-oxo-2-thioxothiazolidin-3-yl)-3-(4-hydroxyphenyl)propanoic acid

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Chemical Name:(S,Z)-2-(5-(4-(2-(2,4-dichlorophenyl)-2-oxoethoxy)benzylidene)-4-oxo-2-thioxothiazolidin-3-yl)-3-(4-hydroxyphenyl)propanoic acid
CAS No.:1393891-31-0
Molecular Formula:C₂₇H₁₉Cl₂NO₆S₂
Molecular Weight:588.489
Hs Code.:

Synonyms:(S,Z)-2-(5-(4-(2-(2,4-dichlorophenyl)-2-oxoethoxy)benzylidene)-4-oxo-2-thioxothiazolidin-3-yl)-3-(4-hydroxyphenyl)propanoic acid

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Chemical Property of (S,Z)-2-(5-(4-(2-(2,4-dichlorophenyl)-2-oxoethoxy)benzylidene)-4-oxo-2-thioxothiazolidin-3-yl)-3-(4-hydroxyphenyl)propanoic acid

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Technology Process of (S,Z)-2-(5-(4-(2-(2,4-dichlorophenyl)-2-oxoethoxy)benzylidene)-4-oxo-2-thioxothiazolidin-3-yl)-3-(4-hydroxyphenyl)propanoic acid

There total 2 articles about (S,Z)-2-(5-(4-(2-(2,4-dichlorophenyl)-2-oxoethoxy)benzylidene)-4-oxo-2-thioxothiazolidin-3-yl)-3-(4-hydroxyphenyl)propanoic acid 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: 53.0%

: 1388204-64-5
(S)-3-(4-hydroxyphenyl)-2-(4-oxo-2-thioxothiazolidin-3-yl)propanoic acid

: 901414-78-6
C₁₅H₁₀Cl₂O₃

: 1393891-31-0
(S,Z)-2-(5-(4-(2-(2,4-dichlorophenyl)-2-oxoethoxy)benzylidene)-4-oxo-2-thioxothiazolidin-3-yl)-3-(4-hydroxyphenyl)propanoic acid

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

Reference yield:

: 2234-16-4
1-(2,4-dichlorophenyl)ethan-1-one

: 1393891-31-0
(S,Z)-2-(5-(4-(2-(2,4-dichlorophenyl)-2-oxoethoxy)benzylidene)-4-oxo-2-thioxothiazolidin-3-yl)-3-(4-hydroxyphenyl)propanoic acid

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