4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4H-isothiazol-3-yl]-2-methyl-benzoic acid

Base Information

Chemical Name:4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4H-isothiazol-3-yl]-2-methyl-benzoic acid
CAS No.:1427274-51-8
Molecular Formula:C₁₈H₁₂Cl₂F₃NO₂S
Molecular Weight:434.266
Hs Code.:

Synonyms:4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4H-isothiazol-3-yl]-2-methyl-benzoic acid

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4H-isothiazol-3-yl]-2-methyl-benzoic acid

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Technology Process of 4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4H-isothiazol-3-yl]-2-methyl-benzoic acid

There total 8 articles about 4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4H-isothiazol-3-yl]-2-methyl-benzoic acid 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: 96.0%

: 1444174-23-5
C₁₉H₁₄Cl₂F₃NO₂S

: 1427274-51-8
4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4H-isothiazol-3-yl]-2-methyl-benzoic acid

Guidance literature:: With water; lithium hydroxide; In tetrahydrofuran; at 20 - 25 ℃; for 16h;

Reference yield:

: 1427274-49-4
4-[5-(3,5-dichloro-phenyl)-5-trifluoromethyl-4,5-dihydro-isothiazol-3-yl]-2-methyl-benzoic acid tert-butyl ester

: 1427274-51-8
4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4H-isothiazol-3-yl]-2-methyl-benzoic acid

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 6h;

Reference yield:

: 1352242-90-0
4-[(E)-3-(3,5-dichloro-phenyl)-4,4,4-trifluoro-but-2-enoyl]-2-methyl-benzoic acid tert-butyl ester

: 1427274-51-8
4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4H-isothiazol-3-yl]-2-methyl-benzoic acid

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / 24 h / 20 °C

2: hydroxylamine-O-sulfonic acid; potassium hydroxide / tetrahydrofuran; water / 0.5 h / 20 °C

3: trifluoroacetic acid / dichloromethane / 6 h / 20 °C

With triethylamine; trifluoroacetic acid; potassium hydroxide; hydroxylamine-O-sulfonic acid; In tetrahydrofuran; dichloromethane; water;