2-(4-(4-chloro-3-(trifluoromethyl)phenoxy)phenethoxy)-1-methyl-5-(2,2,2-trifluoroethyl)pyrimidin-4(1H)-one

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Chemical Name:2-(4-(4-chloro-3-(trifluoromethyl)phenoxy)phenethoxy)-1-methyl-5-(2,2,2-trifluoroethyl)pyrimidin-4(1H)-one
CAS No.:1380428-24-9
Molecular Formula:C₂₂H₁₇ClF₆N₂O₃
Molecular Weight:506.832
Hs Code.:

Synonyms:2-(4-(4-chloro-3-(trifluoromethyl)phenoxy)phenethoxy)-1-methyl-5-(2,2,2-trifluoroethyl)pyrimidin-4(1H)-one

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Chemical Property of 2-(4-(4-chloro-3-(trifluoromethyl)phenoxy)phenethoxy)-1-methyl-5-(2,2,2-trifluoroethyl)pyrimidin-4(1H)-one

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Technology Process of 2-(4-(4-chloro-3-(trifluoromethyl)phenoxy)phenethoxy)-1-methyl-5-(2,2,2-trifluoroethyl)pyrimidin-4(1H)-one

There total 5 articles about 2-(4-(4-chloro-3-(trifluoromethyl)phenoxy)phenethoxy)-1-methyl-5-(2,2,2-trifluoroethyl)pyrimidin-4(1H)-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: 41.3%

: 1380428-23-8
2-(4-(4-chloro-3-(trifluoromethyl)phenoxy)phenethoxy)-5-(2,2,2-trifluoroethyl)pyrimidin-4(1H)-one

: 74-88-4
methyl iodide

: 1380428-24-9
2-(4-(4-chloro-3-(trifluoromethyl)phenoxy)phenethoxy)-1-methyl-5-(2,2,2-trifluoroethyl)pyrimidin-4(1H)-one

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 3h;

Reference yield:

: 516481-95-1
4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}benzaldehyde

: 1380428-24-9
2-(4-(4-chloro-3-(trifluoromethyl)phenoxy)phenethoxy)-1-methyl-5-(2,2,2-trifluoroethyl)pyrimidin-4(1H)-one

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydride / tetrahydrofuran / 0 - 20 °C / Inert atmosphere

1.2: 20 °C

2.1: 9-borabicyclo[3.3.1]nonane / tetrahydrofuran / 0 - 20 °C

2.2: 2 h / 50 °C

3.1: tetrahydrofuran / 3 h / 55 °C / Inert atmosphere

4.1: potassium acetate / toluene / 4 h / Reflux

5.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 3 h / 20 °C

With potassium acetate; sodium hydride; 9-borabicyclo[3.3.1]nonane; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; toluene; 1.1: Wittig Reaction;

Reference yield:

: 6294-93-5
4-chloro-3-trifluoromethylphenol

: 1380428-24-9
2-(4-(4-chloro-3-(trifluoromethyl)phenoxy)phenethoxy)-1-methyl-5-(2,2,2-trifluoroethyl)pyrimidin-4(1H)-one

Guidance literature:: Multi-step reaction with 6 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 0.33 h / 120 °C / Microwave irradiation

2.1: sodium hydride / tetrahydrofuran / 0 - 20 °C / Inert atmosphere

2.2: 20 °C

3.1: 9-borabicyclo[3.3.1]nonane / tetrahydrofuran / 0 - 20 °C

3.2: 2 h / 50 °C

4.1: tetrahydrofuran / 3 h / 55 °C / Inert atmosphere

5.1: potassium acetate / toluene / 4 h / Reflux

6.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 3 h / 20 °C

With potassium acetate; sodium hydride; potassium carbonate; 9-borabicyclo[3.3.1]nonane; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; toluene; 2.1: Wittig Reaction;