1-{2-[2-(2-{2-[2-(2-acetyl-4-bromo-phenoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-5-bromo-phenyl}-ethanone

Base Information

Chemical Name:1-{2-[2-(2-{2-[2-(2-acetyl-4-bromo-phenoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-5-bromo-phenyl}-ethanone
CAS No.:676472-06-3
Molecular Formula:C₂₄H₂₈Br₂O₇
Molecular Weight:588.29
Hs Code.:

Synonyms:1-{2-[2-(2-{2-[2-(2-acetyl-4-bromo-phenoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-5-bromo-phenyl}-ethanone

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Chemical Property of 1-{2-[2-(2-{2-[2-(2-acetyl-4-bromo-phenoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-5-bromo-phenyl}-ethanone

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Technology Process of 1-{2-[2-(2-{2-[2-(2-acetyl-4-bromo-phenoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-5-bromo-phenyl}-ethanone

There total 1 articles about 1-{2-[2-(2-{2-[2-(2-acetyl-4-bromo-phenoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-5-bromo-phenyl}-ethanone 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: 93.0%

: 37860-51-8
tetraethylene glycol di(p-toluenesulfonate)

: 1450-75-5
5-Bromo-2-hydroxyacetophenone

: 676472-06-3
1-{2-[2-(2-{2-[2-(2-acetyl-4-bromo-phenoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-5-bromo-phenyl}-ethanone

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 55 ℃; for 72h;

Reference yield: 100.0%

: 676472-06-3
1-{2-[2-(2-{2-[2-(2-acetyl-4-bromo-phenoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-5-bromo-phenyl}-ethanone

: 676472-09-6
C₂₂H₂₄Br₂O₉

Guidance literature:: With sodium hydroxide; water; bromine; In 1,4-dioxane; for 24h;

Reference yield:

: 676472-06-3
1-{2-[2-(2-{2-[2-(2-acetyl-4-bromo-phenoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-5-bromo-phenyl}-ethanone

: 676472-12-1
C₂₆H₃₂Br₂O₉

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / bromine; NaOH; water / dioxane / 24 h

2: 93 percent / H₂SO₄ / 8 h / Heating

With sodium hydroxide; sulfuric acid; water; bromine; In 1,4-dioxane;