3-benzyl-1-(4-methoxybenzyl)-5-(4-methoxyphenyl)-4-(4-methylsulfanylphenyl)-2-phenyl-3-imidazolinium-4-carboxylate

Base Information

Chemical Name:3-benzyl-1-(4-methoxybenzyl)-5-(4-methoxyphenyl)-4-(4-methylsulfanylphenyl)-2-phenyl-3-imidazolinium-4-carboxylate
CAS No.:1260503-45-4
Molecular Formula:C₃₉H₃₆N₂O₄S
Molecular Weight:628.792
Hs Code.:

Synonyms:3-benzyl-1-(4-methoxybenzyl)-5-(4-methoxyphenyl)-4-(4-methylsulfanylphenyl)-2-phenyl-3-imidazolinium-4-carboxylate

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Chemical Property of 3-benzyl-1-(4-methoxybenzyl)-5-(4-methoxyphenyl)-4-(4-methylsulfanylphenyl)-2-phenyl-3-imidazolinium-4-carboxylate

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Technology Process of 3-benzyl-1-(4-methoxybenzyl)-5-(4-methoxyphenyl)-4-(4-methylsulfanylphenyl)-2-phenyl-3-imidazolinium-4-carboxylate

There total 1 articles about 3-benzyl-1-(4-methoxybenzyl)-5-(4-methoxyphenyl)-4-(4-methylsulfanylphenyl)-2-phenyl-3-imidazolinium-4-carboxylate 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: 75.0%

: 201230-82-2
carbon monoxide

: 385368-37-6
N-benzyl-4-methylthiobenzaldehyde imine

: 3261-60-7
N-(4-methoxybenzylidene)-4-methoxybenzylamine

: 98-88-4
benzoyl chloride

: 1260503-45-4
3-benzyl-1-(4-methoxybenzyl)-5-(4-methoxyphenyl)-4-(4-methylsulfanylphenyl)-2-phenyl-3-imidazolinium-4-carboxylate

Guidance literature:: N-benzyl-4-methylthiobenzaldehyde imine; benzoyl chloride; In acetonitrile; for 0.166667h; Inert atmosphere;

carbon monoxide; With tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; N-ethyl-N,N-diisopropylamine; johnphos; In tetrahydrofuran; acetonitrile; at 45 ℃; under 3040.2 Torr;

N-(4-methoxybenzylidene)-4-methoxybenzylamine; With benzenesulfonic acid; In tetrahydrofuran; acetonitrile; at 20 ℃; for 3h; Inert atmosphere;
DOI:10.1021/jo101858d