tert-butyl 12-(2-(N-(2,4-dimethoxybenzyl)-2,4,5-trifluoro-3-methoxybenzamido)-2-(benzo[d][1,3]dioxol-5-yl)acetamido)dodecylcarbamate

Base Information

Chemical Name:tert-butyl 12-(2-(N-(2,4-dimethoxybenzyl)-2,4,5-trifluoro-3-methoxybenzamido)-2-(benzo[d][1,3]dioxol-5-yl)acetamido)dodecylcarbamate
CAS No.:1026147-16-9
Molecular Formula:C₄₃H₅₆F₃N₃O₉
Molecular Weight:815.928
Hs Code.:

Synonyms:tert-butyl 12-(2-(N-(2,4-dimethoxybenzyl)-2,4,5-trifluoro-3-methoxybenzamido)-2-(benzo[d][1,3]dioxol-5-yl)acetamido)dodecylcarbamate

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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 tert-butyl 12-(2-(N-(2,4-dimethoxybenzyl)-2,4,5-trifluoro-3-methoxybenzamido)-2-(benzo[d][1,3]dioxol-5-yl)acetamido)dodecylcarbamate

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of tert-butyl 12-(2-(N-(2,4-dimethoxybenzyl)-2,4,5-trifluoro-3-methoxybenzamido)-2-(benzo[d][1,3]dioxol-5-yl)acetamido)dodecylcarbamate

There total 1 articles about tert-butyl 12-(2-(N-(2,4-dimethoxybenzyl)-2,4,5-trifluoro-3-methoxybenzamido)-2-(benzo[d][1,3]dioxol-5-yl)acetamido)dodecylcarbamate 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: 74.0%

: 120-57-0,30024-74-9
piperonal

: 1026147-10-3
12-(tert-butoxycarbonylamino)dodecylisocyanide

: 20781-20-8
2,4-Dimethoxybenzylamine

: 112811-65-1
3-methoxy-2,4,5-trifluorobenzoic acid

: 1026147-16-9
tert-butyl 12-(2-(N-(2,4-dimethoxybenzyl)-2,4,5-trifluoro-3-methoxybenzamido)-2-(benzo[d][1,3]dioxol-5-yl)acetamido)dodecylcarbamate

Guidance literature:: piperonal; 2,4-Dimethoxybenzylamine; at 20 ℃; for 0.416667h;

12-(tert-butoxycarbonylamino)dodecylisocyanide; 3-methoxy-2,4,5-trifluorobenzoic acid; at 60 ℃; for 0.6h; Further stages.;
DOI:10.1016/j.tet.2008.02.051