(4E,5Z)-5-[(4-{[2,4-bis(trifluoromethyl)benzyl]oxy}-3-methoxyphenyl)methylidene]-3-ethyl-4-(methylimino)-1,3-thiazolidin-2-one

Base Information

Chemical Name:(4E,5Z)-5-[(4-{[2,4-bis(trifluoromethyl)benzyl]oxy}-3-methoxyphenyl)methylidene]-3-ethyl-4-(methylimino)-1,3-thiazolidin-2-one
CAS No.:1264752-35-3
Molecular Formula:C₂₃H₂₀F₆N₂O₃S
Molecular Weight:518.48
Hs Code.:

Synonyms:(4E,5Z)-5-[(4-{[2,4-bis(trifluoromethyl)benzyl]oxy}-3-methoxyphenyl)methylidene]-3-ethyl-4-(methylimino)-1,3-thiazolidin-2-one

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Chemical Property of (4E,5Z)-5-[(4-{[2,4-bis(trifluoromethyl)benzyl]oxy}-3-methoxyphenyl)methylidene]-3-ethyl-4-(methylimino)-1,3-thiazolidin-2-one

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Technology Process of (4E,5Z)-5-[(4-{[2,4-bis(trifluoromethyl)benzyl]oxy}-3-methoxyphenyl)methylidene]-3-ethyl-4-(methylimino)-1,3-thiazolidin-2-one

There total 6 articles about (4E,5Z)-5-[(4-{[2,4-bis(trifluoromethyl)benzyl]oxy}-3-methoxyphenyl)methylidene]-3-ethyl-4-(methylimino)-1,3-thiazolidin-2-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: 8.0%

: 74-96-4
ethyl bromide

: 1264751-11-2
(5Z)-5-[(4-{[2,4-bis(trifluoromethyl)benzyl]oxy}-3-methoxyphenyl)methylidene]-4-(methylamino)-1,3-thiazol-2(5H)-one

: 1264752-35-3
(4E,5Z)-5-[(4-{[2,4-bis(trifluoromethyl)benzyl]oxy}-3-methoxyphenyl)methylidene]-3-ethyl-4-(methylimino)-1,3-thiazolidin-2-one

Guidance literature:: With potassium carbonate; tetra-(n-butyl)ammonium iodide; In N,N-dimethyl-formamide; at 20 - 60 ℃; for 8h;

Reference yield:

: 796844-14-9
4-((2,4-bis(trifluoromethyl)benzyl)oxy)-3-methoxybenzaldehyde

: 1264752-35-3
(4E,5Z)-5-[(4-{[2,4-bis(trifluoromethyl)benzyl]oxy}-3-methoxyphenyl)methylidene]-3-ethyl-4-(methylimino)-1,3-thiazolidin-2-one

Guidance literature:: Multi-step reaction with 4 steps

1: piperidine / ethanol / 72 h / Reflux

2: Lawessons reagent / toluene / 10 h / Reflux

3: tetrahydrofuran; methanol / 2 h / 100 °C / Microwave irradiation

4: potassium carbonate / tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide / 8 h / 20 - 60 °C

With piperidine; Lawessons reagent; potassium carbonate; tetra-(n-butyl)ammonium iodide; In tetrahydrofuran; methanol; ethanol; N,N-dimethyl-formamide; toluene;

Reference yield:

: 140690-56-8
2,4-bis(trifluoromethyl)benzyl bromide

: 1264752-35-3
(4E,5Z)-5-[(4-{[2,4-bis(trifluoromethyl)benzyl]oxy}-3-methoxyphenyl)methylidene]-3-ethyl-4-(methylimino)-1,3-thiazolidin-2-one

Guidance literature:: Multi-step reaction with 5 steps

1: potassium carbonate / N,N-dimethyl-formamide / 2 h / 20 °C

2: piperidine / ethanol / 72 h / Reflux

3: Lawessons reagent / toluene / 10 h / Reflux

4: tetrahydrofuran; methanol / 2 h / 100 °C / Microwave irradiation

5: potassium carbonate / tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide / 8 h / 20 - 60 °C

With piperidine; Lawessons reagent; potassium carbonate; tetra-(n-butyl)ammonium iodide; In tetrahydrofuran; methanol; ethanol; N,N-dimethyl-formamide; toluene;