4-(3,4-dichlorophenyl)-1-(2-(2,4-difluorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl) propyl)-1H-1,2,4-triazol-5(4H)-one

Base Information

Chemical Name:4-(3,4-dichlorophenyl)-1-(2-(2,4-difluorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl) propyl)-1H-1,2,4-triazol-5(4H)-one
CAS No.:1312809-88-3
Molecular Formula:C₁₉H₁₄Cl₂F₂N₆O₂
Molecular Weight:467.262
Hs Code.:

Synonyms:4-(3,4-dichlorophenyl)-1-(2-(2,4-difluorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl) propyl)-1H-1,2,4-triazol-5(4H)-one

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Chemical Property of 4-(3,4-dichlorophenyl)-1-(2-(2,4-difluorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl) propyl)-1H-1,2,4-triazol-5(4H)-one

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Technology Process of 4-(3,4-dichlorophenyl)-1-(2-(2,4-difluorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl) propyl)-1H-1,2,4-triazol-5(4H)-one

There total 5 articles about 4-(3,4-dichlorophenyl)-1-(2-(2,4-difluorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl) propyl)-1H-1,2,4-triazol-5(4H)-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:

: 1312809-77-0
C₈H₅Cl₂N₃O

: 86386-77-8
1-[2-(2,4-difluorophenyl)-2,3-epoxypropyl]-1H-1,2,4-triazole methanesulfonate

: 1312809-88-3
4-(3,4-dichlorophenyl)-1-(2-(2,4-difluorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl) propyl)-1H-1,2,4-triazol-5(4H)-one

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; for 8h; Reflux;
DOI:10.1016/j.ejmech.2011.02.001

Reference yield:

: 372-18-9
1,3-Difluorobenzene

: 1312809-88-3
4-(3,4-dichlorophenyl)-1-(2-(2,4-difluorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl) propyl)-1H-1,2,4-triazol-5(4H)-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: aluminum (III) chloride / 5 h / 20 °C

2.1: sodium hydrogencarbonate / toluene / 5 h / Reflux

3.1: cetyltrimethylammonim bromide; sodium hydroxide / toluene / 3 h / 60 °C

3.2: 1 h / 0 °C

4.1: potassium carbonate / N,N-dimethyl-formamide / 8 h / Reflux

With aluminum (III) chloride; cetyltrimethylammonim bromide; sodium hydrogencarbonate; potassium carbonate; sodium hydroxide; In N,N-dimethyl-formamide; toluene; 3.1: Corey-Chaykovsky epoxidation;
DOI:10.1016/j.ejmech.2011.02.001

Reference yield:

: 51336-94-8
2-chloro-1-(2,4-dichlorophenyl)ethanone

: 1312809-88-3
4-(3,4-dichlorophenyl)-1-(2-(2,4-difluorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl) propyl)-1H-1,2,4-triazol-5(4H)-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydrogencarbonate / toluene / 5 h / Reflux

2.1: cetyltrimethylammonim bromide; sodium hydroxide / toluene / 3 h / 60 °C

2.2: 1 h / 0 °C

3.1: potassium carbonate / N,N-dimethyl-formamide / 8 h / Reflux

With cetyltrimethylammonim bromide; sodium hydrogencarbonate; potassium carbonate; sodium hydroxide; In N,N-dimethyl-formamide; toluene; 2.1: Corey-Chaykovsky epoxidation;
DOI:10.1016/j.ejmech.2011.02.001