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

Base Information

Chemical Name:(5Z)-5-[(4-{[2,4-bis(trifluoromethyl)benzyl]oxy}-2-bromo-5-methoxyphenyl)methylidene]-4-(methylamino)-1,3-thiazol-2(5H)-one
CAS No.:1264752-32-0
Molecular Formula:C₂₁H₁₅BrF₆N₂O₃S
Molecular Weight:569.322
Hs Code.:

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

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Chemical Property of (5Z)-5-[(4-{[2,4-bis(trifluoromethyl)benzyl]oxy}-2-bromo-5-methoxyphenyl)methylidene]-4-(methylamino)-1,3-thiazol-2(5H)-one

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Technology Process of (5Z)-5-[(4-{[2,4-bis(trifluoromethyl)benzyl]oxy}-2-bromo-5-methoxyphenyl)methylidene]-4-(methylamino)-1,3-thiazol-2(5H)-one

There total 3 articles about (5Z)-5-[(4-{[2,4-bis(trifluoromethyl)benzyl]oxy}-2-bromo-5-methoxyphenyl)methylidene]-4-(methylamino)-1,3-thiazol-2(5H)-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: 90.0%

: 1264753-81-2
4-(methylamino)-1,3-thiazol-2(5H)-one

: 1264753-91-4
4-{[2,4-bis(trifluoromethyl)benzyl]oxy}-2-bromo-5-methoxybenzaldehyde

: 1264752-32-0
(5Z)-5-[(4-{[2,4-bis(trifluoromethyl)benzyl]oxy}-2-bromo-5-methoxyphenyl)methylidene]-4-(methylamino)-1,3-thiazol-2(5H)-one

Guidance literature:: With potassium tert-butylate; In ethanol; for 3h; Inert atmosphere; Reflux;

Reference yield:

: 881-68-5
vanillin acetate

: 1264752-32-0
(5Z)-5-[(4-{[2,4-bis(trifluoromethyl)benzyl]oxy}-2-bromo-5-methoxyphenyl)methylidene]-4-(methylamino)-1,3-thiazol-2(5H)-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: bromine; potassium bromide / water / 8 h / 20 °C

1.2: 16 h / 90 °C

2.1: potassium carbonate / N,N-dimethyl-formamide / 3 h / 60 °C

3.1: potassium tert-butylate / ethanol / 3 h / Inert atmosphere; Reflux

With potassium tert-butylate; bromine; potassium carbonate; potassium bromide; In ethanol; water; N,N-dimethyl-formamide;

Reference yield:

: 60632-40-8
6-bromovanillin

: 1264752-32-0
(5Z)-5-[(4-{[2,4-bis(trifluoromethyl)benzyl]oxy}-2-bromo-5-methoxyphenyl)methylidene]-4-(methylamino)-1,3-thiazol-2(5H)-one

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / N,N-dimethyl-formamide / 3 h / 60 °C

2: potassium tert-butylate / ethanol / 3 h / Inert atmosphere; Reflux

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