2-[4-bromomethyl-5-phenyl-3-(3,4,5-trimethoxybenzoyl)-2-thienyl]-1H-isoindole-1,3(2H)-dione

Base Information

Chemical Name:2-[4-bromomethyl-5-phenyl-3-(3,4,5-trimethoxybenzoyl)-2-thienyl]-1H-isoindole-1,3(2H)-dione
CAS No.:1265047-73-1
Molecular Formula:C₂₉H₂₂BrNO₆S
Molecular Weight:592.467
Hs Code.:

Synonyms:2-[4-bromomethyl-5-phenyl-3-(3,4,5-trimethoxybenzoyl)-2-thienyl]-1H-isoindole-1,3(2H)-dione

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Chemical Property of 2-[4-bromomethyl-5-phenyl-3-(3,4,5-trimethoxybenzoyl)-2-thienyl]-1H-isoindole-1,3(2H)-dione

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Technology Process of 2-[4-bromomethyl-5-phenyl-3-(3,4,5-trimethoxybenzoyl)-2-thienyl]-1H-isoindole-1,3(2H)-dione

There total 5 articles about 2-[4-bromomethyl-5-phenyl-3-(3,4,5-trimethoxybenzoyl)-2-thienyl]-1H-isoindole-1,3(2H)-dione 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: 96.0%

: 901118-65-8
2-[4-methyl-5-phenyl-3-(3,4,5-trimethoxybenzoyl)-2-thienyl]-1H-isoindole-1,3(2H)-dione

: 1265047-73-1
2-[4-bromomethyl-5-phenyl-3-(3,4,5-trimethoxybenzoyl)-2-thienyl]-1H-isoindole-1,3(2H)-dione

Guidance literature:: With N-Bromosuccinimide; dibenzoyl peroxide; In tetrachloromethane; for 5h; Inert atmosphere; Reflux;
DOI:10.2174/157340610793563974

Reference yield:

: 901118-42-1
(2-amino-4-methylthiophen-3-yl)(3,4,5-trimethoxyphenyl)methanone

: 1265047-73-1
2-[4-bromomethyl-5-phenyl-3-(3,4,5-trimethoxybenzoyl)-2-thienyl]-1H-isoindole-1,3(2H)-dione

Guidance literature:: Multi-step reaction with 4 steps

1: acetic acid / 18 h / Reflux; Inert atmosphere

2: N-Bromosuccinimide; dibenzoyl peroxide / benzene / 6 h / Inert atmosphere; Reflux

3: tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium carbonate / toluene / 18 h / 120 °C / Inert atmosphere

4: N-Bromosuccinimide; dibenzoyl peroxide / tetrachloromethane / 5 h / Inert atmosphere; Reflux

With N-Bromosuccinimide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium carbonate; acetic acid; dibenzoyl peroxide; In tetrachloromethane; toluene; benzene; 3: Suzuki coupling;
DOI:10.2174/157340610793563974

Reference yield:

: 901118-53-4
2-[4-methyl-5-bromo-3-(3,4,5-trimethoxybenzoyl)-2-thienyl]-1H-isoindole-1,3(2H)-dione

: 1265047-73-1
2-[4-bromomethyl-5-phenyl-3-(3,4,5-trimethoxybenzoyl)-2-thienyl]-1H-isoindole-1,3(2H)-dione

Guidance literature:: Multi-step reaction with 2 steps

1: tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium carbonate / toluene / 18 h / 120 °C / Inert atmosphere

2: N-Bromosuccinimide; dibenzoyl peroxide / tetrachloromethane / 5 h / Inert atmosphere; Reflux

With N-Bromosuccinimide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium carbonate; dibenzoyl peroxide; In tetrachloromethane; toluene; 1: Suzuki coupling;
DOI:10.2174/157340610793563974