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

Base Information

Chemical Name:ethyl 5-(4-(2,6-dichlorobenzyloxy)phenyl)-2-(furan-2-carboxamido)thiophene-3-carboxylate
CAS No.:1334931-18-8
Molecular Formula:C₂₅H₁₉Cl₂NO₅S
Molecular Weight:516.402
Hs Code.:

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

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

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

There total 6 articles about ethyl 5-(4-(2,6-dichlorobenzyloxy)phenyl)-2-(furan-2-carboxamido)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:

: 88-14-2
2-furanoic acid

: 1334931-18-8
ethyl 5-(4-(2,6-dichlorobenzyloxy)phenyl)-2-(furan-2-carboxamido)thiophene-3-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride / 2 h / Reflux

2: triethylamine / dichloromethane / 20 °C

With thionyl chloride; triethylamine; In dichloromethane;
DOI:10.1016/j.ejmech.2011.05.018

Reference yield:

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

: 1334931-18-8
ethyl 5-(4-(2,6-dichlorobenzyloxy)phenyl)-2-(furan-2-carboxamido)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

: 1334931-18-8
ethyl 5-(4-(2,6-dichlorobenzyloxy)phenyl)-2-(furan-2-carboxamido)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