N-(2-bromo-4,5-dimethoxyphenethyl)-N-(4-methoxybenzyl)-1,4-diphenylbut-3-yn-2-amine

Base Information

Chemical Name:N-(2-bromo-4,5-dimethoxyphenethyl)-N-(4-methoxybenzyl)-1,4-diphenylbut-3-yn-2-amine
CAS No.:1246965-47-8
Molecular Formula:C₃₄H₃₄BrNO₃
Molecular Weight:584.553
Hs Code.:

Synonyms:N-(2-bromo-4,5-dimethoxyphenethyl)-N-(4-methoxybenzyl)-1,4-diphenylbut-3-yn-2-amine

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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-(2-bromo-4,5-dimethoxyphenethyl)-N-(4-methoxybenzyl)-1,4-diphenylbut-3-yn-2-amine

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Technology Process of N-(2-bromo-4,5-dimethoxyphenethyl)-N-(4-methoxybenzyl)-1,4-diphenylbut-3-yn-2-amine

There total 1 articles about N-(2-bromo-4,5-dimethoxyphenethyl)-N-(4-methoxybenzyl)-1,4-diphenylbut-3-yn-2-amine 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%

: 866756-37-8
N-[2-(2-bromo-4,5-dimethoxyphenyl)ethyl]-N-(4-methoxybenzyl)amine

: 536-74-3
phenylacetylene

: 1246965-47-8
N-(2-bromo-4,5-dimethoxyphenethyl)-N-(4-methoxybenzyl)-1,4-diphenylbut-3-yn-2-amine

Guidance literature:: With copper(l) iodide; at 100 ℃; for 0.416667h; regioselective reaction; Microwave irradiation; Inert atmosphere;
DOI:10.1002/ejoc.201000583

Reference yield: 71.0%

: 1246965-47-8
N-(2-bromo-4,5-dimethoxyphenethyl)-N-(4-methoxybenzyl)-1,4-diphenylbut-3-yn-2-amine

: 1246965-68-3
(Z)-2-benzyl-1-benzylidene-7,8-dimethoxy-3-(4-methoxybenzyl)-2,3,4,5-tetrahydro-1H-benzo[d]azepine

Guidance literature:: With tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium formate; In water; N,N-dimethyl-formamide; at 110 ℃; for 0.25h; stereoselective reaction; Inert atmosphere; Microwave irradiation;
DOI:10.1002/ejoc.201000583