C₂₈H₂₆O₈S₂

Base Information

Chemical Name:C₂₈H₂₆O₈S₂
CAS No.:1419172-41-0
Molecular Formula:C₂₈H₂₆O₈S₂
Molecular Weight:554.642
Hs Code.:

C<sub>28</sub>H<sub>26</sub>O<sub>8</sub>S<sub>2</sub>

Synonyms:C₂₈H₂₆O₈S₂

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Chemical Property of C₂₈H₂₆O₈S₂

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Technology Process of C₂₈H₂₆O₈S₂

There total 5 articles about C₂₈H₂₆O₈S₂ 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: 54.0%

: 1419171-84-8
methyl 2-{5-bromo-2-[5-bromo-3-(2-methoxy-2-oxoethyl)thiophen-2-yl]thiophen-3-yl}acetate

: 182344-21-4
(4-hydroxy-3-methoxyphenyl)boronic acid

: 1419172-41-0
C₂₈H₂₆O₈S₂

Guidance literature:: With potassium fluoride; [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride; In methanol; toluene; at 55 ℃; for 1.5h; Inert atmosphere;

Reference yield:

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

: 1419172-41-0
C₂₈H₂₆O₈S₂

Guidance literature:: Multi-step reaction with 4 steps

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

2: potassium fluoride; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; bis(pinacol)diborane / toluene; methanol / 0.5 h / 80 °C / Inert atmosphere; Sealed tube

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

4: [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride; potassium fluoride / toluene; methanol / 1.5 h / 55 °C / Inert atmosphere

With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium fluoride; N-Bromosuccinimide; [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride; acetic acid; bis(pinacol)diborane; In methanol; chloroform; toluene; 4: |Suzuki Coupling;

Reference yield:

: 6964-21-2
thiophen-3-yl-acetic acid

: 1419172-41-0
C₂₈H₂₆O₈S₂

Guidance literature:: Multi-step reaction with 5 steps

1: acetyl chloride / 0 - 20 °C

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

3: potassium fluoride; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; bis(pinacol)diborane / toluene; methanol / 0.5 h / 80 °C / Inert atmosphere; Sealed tube

4: N-Bromosuccinimide; acetic acid / chloroform / 20 °C

5: [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride; potassium fluoride / toluene; methanol / 1.5 h / 55 °C / Inert atmosphere

With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium fluoride; N-Bromosuccinimide; [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride; acetic acid; acetyl chloride; bis(pinacol)diborane; In methanol; chloroform; toluene; 5: |Suzuki Coupling;