ethyl 2-(4-(bis(1-ethyl-1H-indol-3-yl)methyl)phenoxy)-2-methylpropanoate

Base Information

Chemical Name:ethyl 2-(4-(bis(1-ethyl-1H-indol-3-yl)methyl)phenoxy)-2-methylpropanoate
CAS No.:1361044-04-3
Molecular Formula:C₃₃H₃₆N₂O₃
Molecular Weight:508.66
Hs Code.:

Synonyms:ethyl 2-(4-(bis(1-ethyl-1H-indol-3-yl)methyl)phenoxy)-2-methylpropanoate

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Chemical Property of ethyl 2-(4-(bis(1-ethyl-1H-indol-3-yl)methyl)phenoxy)-2-methylpropanoate

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Technology Process of ethyl 2-(4-(bis(1-ethyl-1H-indol-3-yl)methyl)phenoxy)-2-methylpropanoate

There total 4 articles about ethyl 2-(4-(bis(1-ethyl-1H-indol-3-yl)methyl)phenoxy)-2-methylpropanoate 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: 91.0%

: 10604-59-8
N-Ethylindole

: 51336-35-7
α-(4-formylphenoxy)isobutyric acid ethyl ester

: 1361044-04-3
ethyl 2-(4-(bis(1-ethyl-1H-indol-3-yl)methyl)phenoxy)-2-methylpropanoate

Guidance literature:: With iodine; In acetonitrile; at 20 ℃; for 0.5h;
DOI:10.1021/jm201697v

Reference yield:

: 120-72-9
indole

: 1361044-04-3
ethyl 2-(4-(bis(1-ethyl-1H-indol-3-yl)methyl)phenoxy)-2-methylpropanoate

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydride / N,N-dimethyl-formamide / 1 h / 0 °C

2: iodine / acetonitrile / 0.5 h / 20 °C

With iodine; sodium hydride; In N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/jm201697v

Reference yield:

: 123-08-0,65581-83-1
4-hydroxy-benzaldehyde

: 1361044-04-3
ethyl 2-(4-(bis(1-ethyl-1H-indol-3-yl)methyl)phenoxy)-2-methylpropanoate

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / acetonitrile / 3 h / Reflux

2: iodine / acetonitrile / 0.5 h / 20 °C

With iodine; potassium carbonate; In acetonitrile;
DOI:10.1021/jm201697v