2-(5-bromo-3-carboxy-2-hydroxybenzyl)-6-(5-bromo-2-hydroxybenzyl)-4-chlorophenol

Base Information

Chemical Name:2-(5-bromo-3-carboxy-2-hydroxybenzyl)-6-(5-bromo-2-hydroxybenzyl)-4-chlorophenol
CAS No.:196696-23-8
Molecular Formula:C₂₁H₁₅Br₂ClO₅
Molecular Weight:542.608
Hs Code.:

Synonyms:2-(5-bromo-3-carboxy-2-hydroxybenzyl)-6-(5-bromo-2-hydroxybenzyl)-4-chlorophenol

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Chemical Property of 2-(5-bromo-3-carboxy-2-hydroxybenzyl)-6-(5-bromo-2-hydroxybenzyl)-4-chlorophenol

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Technology Process of 2-(5-bromo-3-carboxy-2-hydroxybenzyl)-6-(5-bromo-2-hydroxybenzyl)-4-chlorophenol

There total 1 articles about 2-(5-bromo-3-carboxy-2-hydroxybenzyl)-6-(5-bromo-2-hydroxybenzyl)-4-chlorophenol 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: 95.0%

: 196696-22-7
2-(3-acetyl-5-bromo-2-hydroxybenzyl)-6-(5-bromo-2-hydroxybenzyl)-4-chlorophenol

: 196696-23-8
2-(5-bromo-3-carboxy-2-hydroxybenzyl)-6-(5-bromo-2-hydroxybenzyl)-4-chlorophenol

Guidance literature:: With sodium hydroxide; iodine; potassium iodide; for 0.5h; Heating;

Reference yield: 87.0%

: 196696-23-8
2-(5-bromo-3-carboxy-2-hydroxybenzyl)-6-(5-bromo-2-hydroxybenzyl)-4-chlorophenol

: 196696-08-9
2-(3-Carboxy-2-hydroxybenzyl)-6-(2-hydroxybenzyl)-4-chlorophenol

Guidance literature:: With potassium hydroxide; zinc; for 5h; Heating;

Reference yield:

: 196696-23-8
2-(5-bromo-3-carboxy-2-hydroxybenzyl)-6-(5-bromo-2-hydroxybenzyl)-4-chlorophenol

: (6R,7R)-3-{3-[5-Chloro-2-hydroxy-3-(2-hydroxy-benzyl)-benzyl]-2-hydroxy-benzoyloxymethyl}-8-oxo-7-(2-phenoxy-acetylamino)-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 87 percent / 40percent aq. KOH, Zn / 5 h / Heating

2: 95 percent / NaHCO₃ / dimethylformamide / 4 h

3: 90 percent / CF₃CO₂H / CH₂Cl₂ / 13 h / Ambient temperature

With potassium hydroxide; sodium hydrogencarbonate; trifluoroacetic acid; zinc; In dichloromethane; N,N-dimethyl-formamide;