1-bromo-2-(4-iodophenylamino)ethanesulfonic acid 2,4,6-trichlorophenyl ester

Base Information

Chemical Name:1-bromo-2-(4-iodophenylamino)ethanesulfonic acid 2,4,6-trichlorophenyl ester
CAS No.:1352621-95-4
Molecular Formula:C₁₄H₁₀BrCl₃INO₃S
Molecular Weight:585.472
Hs Code.:

Synonyms:1-bromo-2-(4-iodophenylamino)ethanesulfonic acid 2,4,6-trichlorophenyl ester

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Chemical Property of 1-bromo-2-(4-iodophenylamino)ethanesulfonic acid 2,4,6-trichlorophenyl ester

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Technology Process of 1-bromo-2-(4-iodophenylamino)ethanesulfonic acid 2,4,6-trichlorophenyl ester

There total 3 articles about 1-bromo-2-(4-iodophenylamino)ethanesulfonic acid 2,4,6-trichlorophenyl ester 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: 78.0%

: 1352621-86-3
2,4,6-trichlorophenyl 1-bromoethenesulfonate

: 540-37-4
p-aminoiodobenzene

: 1352621-95-4
1-bromo-2-(4-iodophenylamino)ethanesulfonic acid 2,4,6-trichlorophenyl ester

Guidance literature:: at 100 ℃; for 0.166667h; Neat (no solvent);
DOI:10.1016/j.tetlet.2011.10.093

Reference yield:

: 4790-35-6
ethenesulfonic acid 2,4,6-trichlorophenyl ester

: 1352621-95-4
1-bromo-2-(4-iodophenylamino)ethanesulfonic acid 2,4,6-trichlorophenyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: 2,2'-azobis(isobutyronitrile); bromine / 1,2-dichloro-ethane / 3 h / Reflux

1.2: 1.08 h / -78 - 20 °C

2.1: 0.17 h / 100 °C / Neat (no solvent)

With 2,2'-azobis(isobutyronitrile); bromine; In 1,2-dichloro-ethane; 2.1: Michael addition;
DOI:10.1016/j.tetlet.2011.10.093

Reference yield:

: 88-06-2,67471-29-8
2,4,6-Trichlorophenol

: 1352621-95-4
1-bromo-2-(4-iodophenylamino)ethanesulfonic acid 2,4,6-trichlorophenyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: triethylamine / dichloromethane / -78 - 20 °C

2.1: 2,2'-azobis(isobutyronitrile); bromine / 1,2-dichloro-ethane / 3 h / Reflux

2.2: 1.08 h / -78 - 20 °C

3.1: 0.17 h / 100 °C / Neat (no solvent)

With 2,2'-azobis(isobutyronitrile); bromine; triethylamine; In dichloromethane; 1,2-dichloro-ethane; 3.1: Michael addition;
DOI:10.1016/j.tetlet.2011.10.093