N′-methyl-N′-{2-chloro-5-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]phenyl}-4,4,4-trifluorobutyrohydrazide

Base Information

Chemical Name:N′-methyl-N′-{2-chloro-5-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]phenyl}-4,4,4-trifluorobutyrohydrazide
CAS No.:1237587-42-6
Molecular Formula:C₂₁H₁₆Cl₃F₆N₃O₂
Molecular Weight:562.726
Hs Code.:

Synonyms:N′-methyl-N′-{2-chloro-5-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]phenyl}-4,4,4-trifluorobutyrohydrazide

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Chemical Property of N′-methyl-N′-{2-chloro-5-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]phenyl}-4,4,4-trifluorobutyrohydrazide

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Technology Process of N′-methyl-N′-{2-chloro-5-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]phenyl}-4,4,4-trifluorobutyrohydrazide

There total 11 articles about N′-methyl-N′-{2-chloro-5-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]phenyl}-4,4,4-trifluorobutyrohydrazide 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:

: 406-91-7
4,4,4-trifluorobutanoyl chloride

: 1237587-92-6
N-methyl-N-{2-chloro-5-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]phenyl}hydrazine

: 1237587-42-6
N′-methyl-N′-{2-chloro-5-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]phenyl}-4,4,4-trifluorobutyrohydrazide

Guidance literature:: With triethylamine; In tetrahydrofuran; at 20 ℃;

Reference yield:

: 864725-22-4
1,3-dichloro-5-(3,3,3-trifluoroprop-1-en-2-yl)benzene

: 1237587-42-6
N′-methyl-N′-{2-chloro-5-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]phenyl}-4,4,4-trifluorobutyrohydrazide

Guidance literature:: Multi-step reaction with 8 steps

1.1: N-chloro-succinimide / N,N-dimethyl-formamide / 1 h / 60 °C

1.2: 6 h / 20 °C

2.1: water; acetic acid; iron / ethanol / 0.83 h / 75 °C

3.1: triethylamine / tetrahydrofuran / 0.5 h / 0 °C

4.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.33 h / 20 °C

4.2: 1 h / 20 °C

5.1: potassium carbonate; methanol / 3 h / 20 °C

6.1: hydrogenchloride / water; tetrahydrofuran / 0.17 h / 20 °C

6.2: 1 h / 0 °C

7.1: zinc; water; acetic acid / ethanol; tetrahydrofuran / 3 h / 20 °C

8.1: triethylamine / tetrahydrofuran / 1 h / 20 °C

With hydrogenchloride; methanol; N-chloro-succinimide; water; iron; sodium hydride; potassium carbonate; acetic acid; triethylamine; zinc; In tetrahydrofuran; ethanol; water; N,N-dimethyl-formamide; mineral oil;

Reference yield:

: 66399-01-7
2-chloro-5-hydroxyiminomethylnitrobenzene

: 1237587-42-6
N′-methyl-N′-{2-chloro-5-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]phenyl}-4,4,4-trifluorobutyrohydrazide

Guidance literature:: Multi-step reaction with 8 steps

1.1: N-chloro-succinimide / N,N-dimethyl-formamide / 1 h / 60 °C

1.2: 6 h / 20 °C

2.1: water; acetic acid; iron / ethanol / 0.83 h / 75 °C

3.1: triethylamine / tetrahydrofuran / 0.5 h / 0 °C

4.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.33 h / 20 °C

4.2: 1 h / 20 °C

5.1: potassium carbonate; methanol / 3 h / 20 °C

6.1: hydrogenchloride / water; tetrahydrofuran / 0.17 h / 20 °C

6.2: 1 h / 0 °C

7.1: zinc; water; acetic acid / ethanol; tetrahydrofuran / 3 h / 20 °C

8.1: triethylamine / tetrahydrofuran / 1 h / 20 °C

With hydrogenchloride; methanol; N-chloro-succinimide; water; iron; sodium hydride; potassium carbonate; acetic acid; triethylamine; zinc; In tetrahydrofuran; ethanol; water; N,N-dimethyl-formamide; mineral oil;