(4E,5Z)-5-[(4-{[2,4-bis(trifluoromethyl)benzyl]oxy}-3-methoxyphenyl)methylidene]-3-ethylimidazolidine-2,4-dione 4-(O-methyloxime)

Base Information

Chemical Name:(4E,5Z)-5-[(4-{[2,4-bis(trifluoromethyl)benzyl]oxy}-3-methoxyphenyl)methylidene]-3-ethylimidazolidine-2,4-dione 4-(O-methyloxime)
CAS No.:1264752-51-3
Molecular Formula:C₂₃H₂₁F₆N₃O₄
Molecular Weight:517.428
Hs Code.:

Synonyms:(4E,5Z)-5-[(4-{[2,4-bis(trifluoromethyl)benzyl]oxy}-3-methoxyphenyl)methylidene]-3-ethylimidazolidine-2,4-dione 4-(O-methyloxime)

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Chemical Property of (4E,5Z)-5-[(4-{[2,4-bis(trifluoromethyl)benzyl]oxy}-3-methoxyphenyl)methylidene]-3-ethylimidazolidine-2,4-dione 4-(O-methyloxime)

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Technology Process of (4E,5Z)-5-[(4-{[2,4-bis(trifluoromethyl)benzyl]oxy}-3-methoxyphenyl)methylidene]-3-ethylimidazolidine-2,4-dione 4-(O-methyloxime)

There total 5 articles about (4E,5Z)-5-[(4-{[2,4-bis(trifluoromethyl)benzyl]oxy}-3-methoxyphenyl)methylidene]-3-ethylimidazolidine-2,4-dione 4-(O-methyloxime) 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: 46.0%

: 1264751-38-3
(4Z)-4-[(4-{[2,4-bis(trifluoromethyl)benzyl]oxy}-3-methoxyphenyl)methylidene]-1-ethyl-5-iminoimidazolidin-2-one

: 593-56-6
N-methoxylamine hydrochloride

: 1264752-51-3
(4E,5Z)-5-[(4-{[2,4-bis(trifluoromethyl)benzyl]oxy}-3-methoxyphenyl)methylidene]-3-ethylimidazolidine-2,4-dione 4-(O-methyloxime)

Guidance literature:: (4Z)-4-[(4-{[2,4-bis(trifluoromethyl)benzyl]oxy}-3-methoxyphenyl)methylidene]-1-ethyl-5-iminoimidazolidin-2-one; N-methoxylamine hydrochloride; In methanol; for 5h; Reflux;

With sodium hydrogencarbonate; In methanol; water; ethyl acetate;

Reference yield:

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

: 1264752-51-3
(4E,5Z)-5-[(4-{[2,4-bis(trifluoromethyl)benzyl]oxy}-3-methoxyphenyl)methylidene]-3-ethylimidazolidine-2,4-dione 4-(O-methyloxime)

Guidance literature:: Multi-step reaction with 3 steps

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

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

2.2: 5 h / Reflux

3.1: methanol / 5 h / Reflux

With potassium tert-butylate; potassium carbonate; In methanol; ethanol; N,N-dimethyl-formamide;

Reference yield:

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

: 1264752-51-3
(4E,5Z)-5-[(4-{[2,4-bis(trifluoromethyl)benzyl]oxy}-3-methoxyphenyl)methylidene]-3-ethylimidazolidine-2,4-dione 4-(O-methyloxime)

Guidance literature:: Multi-step reaction with 3 steps

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

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

2.2: 5 h / Reflux

3.1: methanol / 5 h / Reflux

With potassium tert-butylate; potassium carbonate; In methanol; ethanol; N,N-dimethyl-formamide;