4-(4-chloro-3-(trifluoromethyl)phenoxy)-2-fluoro-N-(methylsulfonyl)benzamide

Base Information

Chemical Name:4-(4-chloro-3-(trifluoromethyl)phenoxy)-2-fluoro-N-(methylsulfonyl)benzamide
CAS No.:1354955-65-9
Molecular Formula:C₁₅H₁₀ClF₄NO₄S
Molecular Weight:411.761
Hs Code.:

Synonyms:4-(4-chloro-3-(trifluoromethyl)phenoxy)-2-fluoro-N-(methylsulfonyl)benzamide

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Chemical Property of 4-(4-chloro-3-(trifluoromethyl)phenoxy)-2-fluoro-N-(methylsulfonyl)benzamide

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Technology Process of 4-(4-chloro-3-(trifluoromethyl)phenoxy)-2-fluoro-N-(methylsulfonyl)benzamide

There total 4 articles about 4-(4-chloro-3-(trifluoromethyl)phenoxy)-2-fluoro-N-(methylsulfonyl)benzamide 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: 34.0%

: 3144-09-0
methanesulfonamide

: 1354961-03-7
4-(4-chloro-3-(trifluoromethyl)phenoxy)-2-fluorobenzoic acid

: 1354955-65-9
4-(4-chloro-3-(trifluoromethyl)phenoxy)-2-fluoro-N-(methylsulfonyl)benzamide

Guidance literature:: 4-(4-chloro-3-(trifluoromethyl)phenoxy)-2-fluorobenzoic acid; With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 0.166667h; Inert atmosphere;

methanesulfonamide; In dichloromethane; at 20 ℃; for 16h;

Reference yield:

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

: 1354955-65-9
4-(4-chloro-3-(trifluoromethyl)phenoxy)-2-fluoro-N-(methylsulfonyl)benzamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium carbonate / dimethyl sulfoxide / 16 h / 110 °C / Inert atmosphere

2.1: water; lithium hydroxide / tetrahydrofuran / 16 h / 20 °C

3.1: dmap; N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 0.17 h / 20 °C / Inert atmosphere

3.2: 16 h / 20 °C

With dmap; water; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; lithium hydroxide; In tetrahydrofuran; dichloromethane; dimethyl sulfoxide;

Reference yield:

: 108928-00-3
ethyl 2,4-di-fluorobenzoate

: 1354955-65-9
4-(4-chloro-3-(trifluoromethyl)phenoxy)-2-fluoro-N-(methylsulfonyl)benzamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium carbonate / dimethyl sulfoxide / 16 h / 110 °C / Inert atmosphere

2.1: water; lithium hydroxide / tetrahydrofuran / 16 h / 20 °C

3.1: dmap; N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 0.17 h / 20 °C / Inert atmosphere

3.2: 16 h / 20 °C

With dmap; water; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; lithium hydroxide; In tetrahydrofuran; dichloromethane; dimethyl sulfoxide;