N-butyl-N-[2-fluoro-4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)phenyl]-2-iodobenzamide

Base Information

Chemical Name:N-butyl-N-[2-fluoro-4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)phenyl]-2-iodobenzamide
CAS No.:1307740-96-0
Molecular Formula:C₂₀H₁₇F₇INO₂
Molecular Weight:563.254
Hs Code.:

Synonyms:N-butyl-N-[2-fluoro-4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)phenyl]-2-iodobenzamide

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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 N-butyl-N-[2-fluoro-4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)phenyl]-2-iodobenzamide

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Technology Process of N-butyl-N-[2-fluoro-4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)phenyl]-2-iodobenzamide

There total 2 articles about N-butyl-N-[2-fluoro-4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)phenyl]-2-iodobenzamide 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: 87.0%

: 609-67-6
2-Iodobenzoyl chloride

: 1307740-84-6
2-(4-butylamino-3-fluorophenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol

: 1307740-96-0
N-butyl-N-[2-fluoro-4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)phenyl]-2-iodobenzamide

Guidance literature:: With triethylamine; In dichloromethane; at 0 ℃; for 3h;
DOI:10.1016/j.bmc.2011.03.002

Reference yield:

: 581798-35-8
butyl-(2-fluoro-phenyl)amine

: 1307740-96-0
N-butyl-N-[2-fluoro-4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)phenyl]-2-iodobenzamide

Guidance literature:: Multi-step reaction with 2 steps

1: toluene-4-sulfonic acid / toluene / 10 h / 120 °C

2: triethylamine / dichloromethane / 3 h / 0 °C

With toluene-4-sulfonic acid; triethylamine; In dichloromethane; toluene;
DOI:10.1016/j.bmc.2011.03.002