1-<2-<2-(4-chloromethylphenoxy)ethoxy>ethoxy>-4-benzene

Base Information

Chemical Name:1-<2-<2-(4-chloromethylphenoxy)ethoxy>ethoxy>-4-benzene
CAS No.:143998-19-0
Molecular Formula:C₄₈H₅₇ClO₃
Molecular Weight:717.432
Hs Code.:

1-<2-<2-(4-chloromethylphenoxy)ethoxy>ethoxy>-4-<tris(4-tert-butylphenyl)methyl>benzene

Synonyms:1-<2-<2-(4-chloromethylphenoxy)ethoxy>ethoxy>-4-benzene

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Chemical Property of 1-<2-<2-(4-chloromethylphenoxy)ethoxy>ethoxy>-4-benzene

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Technology Process of 1-<2-<2-(4-chloromethylphenoxy)ethoxy>ethoxy>-4-benzene

There total 9 articles about 1-<2-<2-(4-chloromethylphenoxy)ethoxy>ethoxy>-4-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: 90.0%

: 143998-23-6
1-<2-<2-(4-hydroxymethylphenoxy)ethoxy>ethoxy>-4-benzene

: 143998-19-0
1-<2-<2-(4-chloromethylphenoxy)ethoxy>ethoxy>-4-benzene

Guidance literature:: With N-chloro-succinimide; In tetrahydrofuran;
DOI:10.1039/c39920001124

Reference yield:

: 143998-21-4
mono-p-phenyl ether of di(ethylene glycol)

: 143998-19-0
1-<2-<2-(4-chloromethylphenoxy)ethoxy>ethoxy>-4-benzene

Guidance literature:: Multi-step reaction with 3 steps

1: 78 percent / 30percent aq. NaOH, benzyltriethylammonium bromide / CH₂Cl₂ / 12 h / Ambient temperature

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

3: N-chlorosuccinimide, Ph₃P / tetrahydrofuran / 15 h / Ambient temperature

With sodium hydroxide; N-chloro-succinimide; benzyltriethylammonium bromide; potassium carbonate; triphenylphosphine; In tetrahydrofuran; dichloromethane;
DOI:10.1021/ja954334d

Reference yield:

: 143998-22-5
1-<2-<2-(toluene-p-sulfonyl)ethoxy>ethoxy>-4-benzene

: 143998-19-0
1-<2-<2-(4-chloromethylphenoxy)ethoxy>ethoxy>-4-benzene

Guidance literature:: Multi-step reaction with 2 steps

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

2: N-chlorosuccinimide, Ph₃P / tetrahydrofuran / 15 h / Ambient temperature

With N-chloro-succinimide; potassium carbonate; triphenylphosphine; In tetrahydrofuran;
DOI:10.1021/ja954334d