4-{4-[(Z)-(1-ethyl-5-imino-3-methyl-2-oxoimidazolidin-4-ylidene)methyl]-2-methoxyphenoxy}-3-(trifluoromethyl)benzonitrile

Base Information

Chemical Name:4-{4-[(Z)-(1-ethyl-5-imino-3-methyl-2-oxoimidazolidin-4-ylidene)methyl]-2-methoxyphenoxy}-3-(trifluoromethyl)benzonitrile
CAS No.:1264752-49-9
Molecular Formula:C₂₂H₁₉F₃N₄O₃
Molecular Weight:444.413
Hs Code.:

Synonyms:4-{4-[(Z)-(1-ethyl-5-imino-3-methyl-2-oxoimidazolidin-4-ylidene)methyl]-2-methoxyphenoxy}-3-(trifluoromethyl)benzonitrile

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Chemical Property of 4-{4-[(Z)-(1-ethyl-5-imino-3-methyl-2-oxoimidazolidin-4-ylidene)methyl]-2-methoxyphenoxy}-3-(trifluoromethyl)benzonitrile

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Technology Process of 4-{4-[(Z)-(1-ethyl-5-imino-3-methyl-2-oxoimidazolidin-4-ylidene)methyl]-2-methoxyphenoxy}-3-(trifluoromethyl)benzonitrile

There total 6 articles about 4-{4-[(Z)-(1-ethyl-5-imino-3-methyl-2-oxoimidazolidin-4-ylidene)methyl]-2-methoxyphenoxy}-3-(trifluoromethyl)benzonitrile 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: 89.0%

: 1264751-33-8
4-{4-[(Z)-(1-ethyl-5-imino-2-oxoimidazolidin-4-ylidene)methyl]-2-methoxyphenoxy}-3-(trifluoromethyl)benzonitrile

: 74-88-4
methyl iodide

: 1264752-49-9
4-{4-[(Z)-(1-ethyl-5-imino-3-methyl-2-oxoimidazolidin-4-ylidene)methyl]-2-methoxyphenoxy}-3-(trifluoromethyl)benzonitrile

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 60 ℃; for 2h;

Reference yield:

: 121-33-5,8014-42-4
vanillin

: 1264752-49-9
4-{4-[(Z)-(1-ethyl-5-imino-3-methyl-2-oxoimidazolidin-4-ylidene)methyl]-2-methoxyphenoxy}-3-(trifluoromethyl)benzonitrile

Guidance literature:: Multi-step reaction with 5 steps

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

1.2: 72 h / 20 °C

2.1: potassium tert-butylate / ethanol / 0.5 h / 20 °C

2.2: 4 h / Reflux

3.1: trifluoroacetic acid / 1 h / 20 °C

3.3: pH 6

4.1: caesium carbonate / N,N-dimethyl-formamide / 20 h / 80 °C

5.1: potassium carbonate / N,N-dimethyl-formamide / 2 h / 60 °C

With potassium tert-butylate; potassium carbonate; caesium carbonate; trifluoroacetic acid; In ethanol; N,N-dimethyl-formamide;

Reference yield:

: 129047-38-7
3-methoxy 4-((4-methoxybenzyl)oxy)benzaldehyde

: 1264752-49-9
4-{4-[(Z)-(1-ethyl-5-imino-3-methyl-2-oxoimidazolidin-4-ylidene)methyl]-2-methoxyphenoxy}-3-(trifluoromethyl)benzonitrile

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium tert-butylate / ethanol / 0.5 h / 20 °C

1.2: 4 h / Reflux

2.1: trifluoroacetic acid / 1 h / 20 °C

2.3: pH 6

3.1: caesium carbonate / N,N-dimethyl-formamide / 20 h / 80 °C

4.1: potassium carbonate / N,N-dimethyl-formamide / 2 h / 60 °C

With potassium tert-butylate; potassium carbonate; caesium carbonate; trifluoroacetic acid; In ethanol; N,N-dimethyl-formamide;