5-[4-(carboxymethyl)-5-{3-[3-(carboxymethyl)-5-(5-carboxythiophen-2-yl)thiophen-2-yl]phenyl}thiophen-2-yl]thiophene-2-carboxylic acid

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Chemical Name:5-[4-(carboxymethyl)-5-{3-[3-(carboxymethyl)-5-(5-carboxythiophen-2-yl)thiophen-2-yl]phenyl}thiophen-2-yl]thiophene-2-carboxylic acid
CAS No.:1419169-94-0
Molecular Formula:C₂₈H₁₈O₈S₄
Molecular Weight:610.71
Hs Code.:

Synonyms:5-[4-(carboxymethyl)-5-{3-[3-(carboxymethyl)-5-(5-carboxythiophen-2-yl)thiophen-2-yl]phenyl}thiophen-2-yl]thiophene-2-carboxylic acid

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Chemical Property of 5-[4-(carboxymethyl)-5-{3-[3-(carboxymethyl)-5-(5-carboxythiophen-2-yl)thiophen-2-yl]phenyl}thiophen-2-yl]thiophene-2-carboxylic acid

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Technology Process of 5-[4-(carboxymethyl)-5-{3-[3-(carboxymethyl)-5-(5-carboxythiophen-2-yl)thiophen-2-yl]phenyl}thiophen-2-yl]thiophene-2-carboxylic acid

There total 6 articles about 5-[4-(carboxymethyl)-5-{3-[3-(carboxymethyl)-5-(5-carboxythiophen-2-yl)thiophen-2-yl]phenyl}thiophen-2-yl]thiophene-2-carboxylic acid 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: 72.0%

: (x)C₆H₁₅N*C₃₀H₂₂O₈S₄

: 1419169-94-0
5-[4-(carboxymethyl)-5-{3-[3-(carboxymethyl)-5-(5-carboxythiophen-2-yl)thiophen-2-yl]phenyl}thiophen-2-yl]thiophene-2-carboxylic acid

Guidance literature:: With sodium hydroxide; In 1,4-dioxane; at 20 ℃; for 18h;

Reference yield:

: 58414-52-1
thiophen-3-yl-acetic acid methyl ester

: 1419169-94-0
5-[4-(carboxymethyl)-5-{3-[3-(carboxymethyl)-5-(5-carboxythiophen-2-yl)thiophen-2-yl]phenyl}thiophen-2-yl]thiophene-2-carboxylic acid

Guidance literature:: Multi-step reaction with 5 steps

1: N-Bromosuccinimide; acetic acid / chloroform / 72 h / 0 - 20 °C

2: potassium carbonate; [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride / toluene; methanol / 1 h / 60 °C / Inert atmosphere

3: N-Bromosuccinimide; acetic acid / chloroform / 18 h / 0 - 20 °C

4: potassium carbonate; [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride / toluene; methanol / 2 h / 45 °C / Inert atmosphere

5: sodium hydroxide / 1,4-dioxane / 18 h / 20 °C

With N-Bromosuccinimide; [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride; potassium carbonate; acetic acid; sodium hydroxide; In 1,4-dioxane; methanol; chloroform; toluene; 2: |Suzuki Coupling / 4: |Suzuki Coupling;

Reference yield:

: 1419171-74-6
methyl 2-(2-{3-[3-(2-methoxy-2-oxoethyl)thiophen-2-yl]phenyl}thiophen-3-yl)acetate

: 1419169-94-0
5-[4-(carboxymethyl)-5-{3-[3-(carboxymethyl)-5-(5-carboxythiophen-2-yl)thiophen-2-yl]phenyl}thiophen-2-yl]thiophene-2-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1: N-Bromosuccinimide; acetic acid / chloroform / 18 h / 0 - 20 °C

2: potassium carbonate; [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride / toluene; methanol / 2 h / 45 °C / Inert atmosphere

3: sodium hydroxide / 1,4-dioxane / 18 h / 20 °C

With N-Bromosuccinimide; [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride; potassium carbonate; acetic acid; sodium hydroxide; In 1,4-dioxane; methanol; chloroform; toluene; 2: |Suzuki Coupling;