3-(4-hydroxyphenyl)-2-thioxo-5-{4-[(1,3,3-trimethyl-1,3-dihydroindol-2-ylidenemethyl)azo]benzylidene}thiazolidin-4-one

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Chemical Name:3-(4-hydroxyphenyl)-2-thioxo-5-{4-[(1,3,3-trimethyl-1,3-dihydroindol-2-ylidenemethyl)azo]benzylidene}thiazolidin-4-one
CAS No.:1268494-92-3
Molecular Formula:C₂₈H₂₄N₄O₂S₂
Molecular Weight:512.656
Hs Code.:

Synonyms:3-(4-hydroxyphenyl)-2-thioxo-5-{4-[(1,3,3-trimethyl-1,3-dihydroindol-2-ylidenemethyl)azo]benzylidene}thiazolidin-4-one

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Chemical Property of 3-(4-hydroxyphenyl)-2-thioxo-5-{4-[(1,3,3-trimethyl-1,3-dihydroindol-2-ylidenemethyl)azo]benzylidene}thiazolidin-4-one

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Technology Process of 3-(4-hydroxyphenyl)-2-thioxo-5-{4-[(1,3,3-trimethyl-1,3-dihydroindol-2-ylidenemethyl)azo]benzylidene}thiazolidin-4-one

There total 4 articles about 3-(4-hydroxyphenyl)-2-thioxo-5-{4-[(1,3,3-trimethyl-1,3-dihydroindol-2-ylidenemethyl)azo]benzylidene}thiazolidin-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: 75.0%

: 1268494-96-7
4-[(1,3,3-trimethyl-1,3-dihydroindol-2-ylidenemethyl)azo]benzaldehyde

: 21346-21-4
3-(4-hydroxyphenyl)-2-thioxothiazolidin-4-one

: 1268494-92-3
3-(4-hydroxyphenyl)-2-thioxo-5-{4-[(1,3,3-trimethyl-1,3-dihydroindol-2-ylidenemethyl)azo]benzylidene}thiazolidin-4-one

Guidance literature:: With triethylamine; In methanol; for 4h; Reflux;
DOI:10.1016/j.dyepig.2012.04.022

Reference yield:

: 79482-19-2
C₇H₅N₂O⁽¹⁺⁾*HO₄S^(1-)

: 1268494-92-3
3-(4-hydroxyphenyl)-2-thioxo-5-{4-[(1,3,3-trimethyl-1,3-dihydroindol-2-ylidenemethyl)azo]benzylidene}thiazolidin-4-one

Guidance literature:: Multi-step reaction with 2 steps

1: acetic acid / 2 h / 0 - 20 °C

2: triethylamine / methanol / 4 h / Reflux

With triethylamine; In methanol; acetic acid;
DOI:10.1016/j.dyepig.2012.04.022

Reference yield:

: 118-12-7
1,3,3-Trimethyl-2-methyleneindoline

: 1268494-92-3
3-(4-hydroxyphenyl)-2-thioxo-5-{4-[(1,3,3-trimethyl-1,3-dihydroindol-2-ylidenemethyl)azo]benzylidene}thiazolidin-4-one

Guidance literature:: Multi-step reaction with 2 steps

1: acetic acid / 2 h / 0 - 20 °C

2: triethylamine / methanol / 4 h / Reflux

With triethylamine; In methanol; acetic acid;
DOI:10.1016/j.dyepig.2012.04.022