ethyl 5-(4-(2,6-dichlorobenzyloxy)phenyl)-2-(3-chlorobenzamido)thiophene-3-carboxylate

Base Information

Chemical Name:ethyl 5-(4-(2,6-dichlorobenzyloxy)phenyl)-2-(3-chlorobenzamido)thiophene-3-carboxylate
CAS No.:1334931-03-1
Molecular Formula:C₂₇H₂₀Cl₃NO₄S
Molecular Weight:560.885
Hs Code.:

Synonyms:ethyl 5-(4-(2,6-dichlorobenzyloxy)phenyl)-2-(3-chlorobenzamido)thiophene-3-carboxylate

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Chemical Property of ethyl 5-(4-(2,6-dichlorobenzyloxy)phenyl)-2-(3-chlorobenzamido)thiophene-3-carboxylate

Chemical Property:

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Technology Process of ethyl 5-(4-(2,6-dichlorobenzyloxy)phenyl)-2-(3-chlorobenzamido)thiophene-3-carboxylate

There total 5 articles about ethyl 5-(4-(2,6-dichlorobenzyloxy)phenyl)-2-(3-chlorobenzamido)thiophene-3-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:

: 1334930-83-4
2-(4-(2,6-dichlorobenzyloxy)phenyl)ethanol

: 1334931-03-1
ethyl 5-(4-(2,6-dichlorobenzyloxy)phenyl)-2-(3-chlorobenzamido)thiophene-3-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: sodium bromite trihydrate; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; sodium hydrogencarbonate / dichloromethane; water / 0.5 h / 0 - 20 °C / pH 8.6

2: sulfur; triethylamine / ethanol / 60 °C

3: triethylamine / dichloromethane / 20 °C

With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; sodium bromite trihydrate; sodium hydrogencarbonate; sulfur; triethylamine; In ethanol; dichloromethane; water;
DOI:10.1016/j.ejmech.2011.05.018

Reference yield:

: 1334930-88-9
2-(4-(2,6-dichlorobenzyloxy)phenyl)acetaldehyde

: 1334931-03-1
ethyl 5-(4-(2,6-dichlorobenzyloxy)phenyl)-2-(3-chlorobenzamido)thiophene-3-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: sulfur; triethylamine / ethanol / 60 °C

2: triethylamine / dichloromethane / 20 °C

With sulfur; triethylamine; In ethanol; dichloromethane;
DOI:10.1016/j.ejmech.2011.05.018

Reference yield:

: 501-94-0
p-hydroxyphenethyl alcohol

: 1334931-03-1
ethyl 5-(4-(2,6-dichlorobenzyloxy)phenyl)-2-(3-chlorobenzamido)thiophene-3-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / acetone / 24 h / Reflux

2: sodium bromite trihydrate; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; sodium hydrogencarbonate / dichloromethane; water / 0.5 h / 0 - 20 °C / pH 8.6

3: sulfur; triethylamine / ethanol / 60 °C

4: triethylamine / dichloromethane / 20 °C

With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; sodium bromite trihydrate; sodium hydrogencarbonate; potassium carbonate; sulfur; triethylamine; In ethanol; dichloromethane; water; acetone;
DOI:10.1016/j.ejmech.2011.05.018