{4-[2-(2-{4-[Bis-(4-tert-butyl-phenyl)-p-tolyl-methyl]-phenoxy}-ethoxy)-ethoxy]-phenyl}-methanol

Base Information

Chemical Name:{4-[2-(2-{4-[Bis-(4-tert-butyl-phenyl)-p-tolyl-methyl]-phenoxy}-ethoxy)-ethoxy]-phenyl}-methanol
CAS No.:177609-55-1
Molecular Formula:C₄₅H₅₂O₄
Molecular Weight:656.905
Hs Code.:

Synonyms:{4-[2-(2-{4-[Bis-(4-tert-butyl-phenyl)-p-tolyl-methyl]-phenoxy}-ethoxy)-ethoxy]-phenyl}-methanol

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Chemical Property of {4-[2-(2-{4-[Bis-(4-tert-butyl-phenyl)-p-tolyl-methyl]-phenoxy}-ethoxy)-ethoxy]-phenyl}-methanol

Chemical Property:

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Technology Process of {4-[2-(2-{4-[Bis-(4-tert-butyl-phenyl)-p-tolyl-methyl]-phenoxy}-ethoxy)-ethoxy]-phenyl}-methanol

There total 7 articles about {4-[2-(2-{4-[Bis-(4-tert-butyl-phenyl)-p-tolyl-methyl]-phenoxy}-ethoxy)-ethoxy]-phenyl}-methanol 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:

: 177609-51-7
2-(2-{4-[Bis-(4-tert-butyl-phenyl)-p-tolyl-methyl]-phenoxy}-ethoxy)-ethanol

: 177609-55-1
{4-[2-(2-{4-[Bis-(4-tert-butyl-phenyl)-p-tolyl-methyl]-phenoxy}-ethoxy)-ethoxy]-phenyl}-methanol

Guidance literature:: Multi-step reaction with 2 steps

1: 60 percent / 30percent aq. NaOH, benzyltriethylammonium bromide / CH₂Cl₂ / 12 h / Ambient temperature

2: 1.) K₂CO₃ / 1.) acetonitrile, reflux, 30 min, 2.) acetonitrile, reflux, 48 h

With sodium hydroxide; benzyltriethylammonium bromide; potassium carbonate; In dichloromethane;
DOI:10.1021/ja954334d

Reference yield:

: Potassium; 4-[bis-(4-tert-butyl-phenyl)-p-tolyl-methyl]-phenolate

: 177609-55-1
{4-[2-(2-{4-[Bis-(4-tert-butyl-phenyl)-p-tolyl-methyl]-phenoxy}-ethoxy)-ethoxy]-phenyl}-methanol

Guidance literature:: Multi-step reaction with 3 steps

1: 83 percent / K₂CO₃ / acetonitrile / 120 h / Heating

2: 60 percent / 30percent aq. NaOH, benzyltriethylammonium bromide / CH₂Cl₂ / 12 h / Ambient temperature

3: 1.) K₂CO₃ / 1.) acetonitrile, reflux, 30 min, 2.) acetonitrile, reflux, 48 h

With sodium hydroxide; benzyltriethylammonium bromide; potassium carbonate; In dichloromethane; acetonitrile;
DOI:10.1021/ja954334d