4,5-diiodo-1,2-bis[2-[2-[2-[[(4-tosyl)sulfonyl]oxy]-ethoxy]ethoxy]ethoxy]benzene

Base Information

Chemical Name:4,5-diiodo-1,2-bis[2-[2-[2-[[(4-tosyl)sulfonyl]oxy]-ethoxy]ethoxy]ethoxy]benzene
CAS No.:875325-90-9
Molecular Formula:C₃₂H₄₀I₂O₁₂S₂
Molecular Weight:934.603
Hs Code.:

Synonyms:4,5-diiodo-1,2-bis[2-[2-[2-[[(4-tosyl)sulfonyl]oxy]-ethoxy]ethoxy]ethoxy]benzene

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 4,5-diiodo-1,2-bis[2-[2-[2-[[(4-tosyl)sulfonyl]oxy]-ethoxy]ethoxy]ethoxy]benzene

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Technology Process of 4,5-diiodo-1,2-bis[2-[2-[2-[[(4-tosyl)sulfonyl]oxy]-ethoxy]ethoxy]ethoxy]benzene

There total 8 articles about 4,5-diiodo-1,2-bis[2-[2-[2-[[(4-tosyl)sulfonyl]oxy]-ethoxy]ethoxy]ethoxy]benzene 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: 80.0%

: 875325-89-6
4,5-diodo-1,2-bis[2-[2-(2-hydroxyethoxy)ethoxy]-ethoxy]benzene

: 98-59-9
p-toluenesulfonyl chloride

: 875325-90-9
4,5-diiodo-1,2-bis[2-[2-[2-[[(4-tosyl)sulfonyl]oxy]-ethoxy]ethoxy]ethoxy]benzene

Guidance literature:: With dmap; triethylamine; In dichloromethane; at 0 ℃; for 2h;
DOI:10.1016/j.tetlet.2005.10.147

Reference yield:

: 875325-88-5
5,6-diiodo-2,2-dimethylbenzo[1,3]dixole

: 875325-90-9
4,5-diiodo-1,2-bis[2-[2-[2-[[(4-tosyl)sulfonyl]oxy]-ethoxy]ethoxy]ethoxy]benzene

Guidance literature:: Multi-step reaction with 3 steps

1: 94 percent / aq. HCl; AcOH / 2 h / Heating

2: 61 percent / K₂CO₃ / acetone / Heating

3: 80 percent / DMAP; Et₃N / CH₂Cl₂ / 2 h / 0 °C

With hydrogenchloride; dmap; potassium carbonate; acetic acid; triethylamine; In dichloromethane; acetone;
DOI:10.1016/j.tetlet.2005.10.147

Reference yield:

: 14005-14-2
2,2-dimethyl-1,3-benzodioxole

: 875325-90-9
4,5-diiodo-1,2-bis[2-[2-[2-[[(4-tosyl)sulfonyl]oxy]-ethoxy]ethoxy]ethoxy]benzene

Guidance literature:: Multi-step reaction with 4 steps

1: 86 percent / iodine; mercuric acetate / CH₂Cl₂ / 20 °C

2: 94 percent / aq. HCl; AcOH / 2 h / Heating

3: 61 percent / K₂CO₃ / acetone / Heating

4: 80 percent / DMAP; Et₃N / CH₂Cl₂ / 2 h / 0 °C

With hydrogenchloride; dmap; mercury(II) diacetate; iodine; potassium carbonate; acetic acid; triethylamine; In dichloromethane; acetone;
DOI:10.1016/j.tetlet.2005.10.147