ethyl 2-(2,5-dimethyl-4-(1-(3-(4-methyl-5-oxo-1-(4-trifluoromethyl-phenyl)-4,5-dihydrogen-1H-1,2,4-triazolyl))-benzylthio)-phenoxy)-acetate

Base Information

Chemical Name:ethyl 2-(2,5-dimethyl-4-(1-(3-(4-methyl-5-oxo-1-(4-trifluoromethyl-phenyl)-4,5-dihydrogen-1H-1,2,4-triazolyl))-benzylthio)-phenoxy)-acetate
CAS No.:1207268-89-0
Molecular Formula:C₂₉H₂₈F₃N₃O₄S
Molecular Weight:571.62
Hs Code.:

Synonyms:ethyl 2-(2,5-dimethyl-4-(1-(3-(4-methyl-5-oxo-1-(4-trifluoromethyl-phenyl)-4,5-dihydrogen-1H-1,2,4-triazolyl))-benzylthio)-phenoxy)-acetate

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Chemical Property of ethyl 2-(2,5-dimethyl-4-(1-(3-(4-methyl-5-oxo-1-(4-trifluoromethyl-phenyl)-4,5-dihydrogen-1H-1,2,4-triazolyl))-benzylthio)-phenoxy)-acetate

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Technology Process of ethyl 2-(2,5-dimethyl-4-(1-(3-(4-methyl-5-oxo-1-(4-trifluoromethyl-phenyl)-4,5-dihydrogen-1H-1,2,4-triazolyl))-benzylthio)-phenoxy)-acetate

There total 7 articles about ethyl 2-(2,5-dimethyl-4-(1-(3-(4-methyl-5-oxo-1-(4-trifluoromethyl-phenyl)-4,5-dihydrogen-1H-1,2,4-triazolyl))-benzylthio)-phenoxy)-acetate 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:

: 1207269-18-8
3-(1'-bromo-benzyl)-4-methyl-1-(4-trifluoromethyl)phenyl-1H-1,2,4-triazole-5(4H)-one

: 106949-90-0
2,5-dimethyl-4-hydroxy-mercaptobenzene

: 105-36-2
ethyl bromoacetate

: 1207268-89-0
ethyl 2-(2,5-dimethyl-4-(1-(3-(4-methyl-5-oxo-1-(4-trifluoromethyl-phenyl)-4,5-dihydrogen-1H-1,2,4-triazolyl))-benzylthio)-phenoxy)-acetate

Guidance literature:: 3-(1'-bromo-benzyl)-4-methyl-1-(4-trifluoromethyl)phenyl-1H-1,2,4-triazole-5(4H)-one; 2,5-dimethyl-4-hydroxy-mercaptobenzene; With potassium carbonate; In acetonitrile; at 20 ℃; for 4h;

ethyl bromoacetate; With potassium carbonate; In acetonitrile; at 20 ℃;

Reference yield:

: 101-41-7
benzeneacetic acid methyl ester

: 1207268-89-0
ethyl 2-(2,5-dimethyl-4-(1-(3-(4-methyl-5-oxo-1-(4-trifluoromethyl-phenyl)-4,5-dihydrogen-1H-1,2,4-triazolyl))-benzylthio)-phenoxy)-acetate

Guidance literature:: Multi-step reaction with 5 steps

1.1: water / 3 h / Reflux

2.1: trichlorophosphate / toluene / 5 h / 80 - 90 °C

3.1: dmap / tetrahydrofuran / 12 h / 20 °C

4.1: dibenzoyl peroxide; N-Bromosuccinimide / chloroform / 12 h / Reflux

5.1: potassium carbonate / acetonitrile / 4 h / 20 °C

5.2: 20 °C

With dmap; N-Bromosuccinimide; potassium carbonate; trichlorophosphate; dibenzoyl peroxide; In tetrahydrofuran; chloroform; water; toluene; acetonitrile;

Reference yield:

: 103-82-2
phenylacetic acid

: 1207268-89-0
ethyl 2-(2,5-dimethyl-4-(1-(3-(4-methyl-5-oxo-1-(4-trifluoromethyl-phenyl)-4,5-dihydrogen-1H-1,2,4-triazolyl))-benzylthio)-phenoxy)-acetate

Guidance literature:: Multi-step reaction with 6 steps

1.1: sulfuric acid / 2 h / Reflux

2.1: water / 3 h / Reflux

3.1: trichlorophosphate / toluene / 5 h / 80 - 90 °C

4.1: dmap / tetrahydrofuran / 12 h / 20 °C

5.1: dibenzoyl peroxide; N-Bromosuccinimide / chloroform / 12 h / Reflux

6.1: potassium carbonate / acetonitrile / 4 h / 20 °C

6.2: 20 °C

With dmap; N-Bromosuccinimide; sulfuric acid; potassium carbonate; trichlorophosphate; dibenzoyl peroxide; In tetrahydrofuran; chloroform; water; toluene; acetonitrile;