1,4-bis<2-<2-<2-<2-<<2-<2-<2-<2-(4-benzyloxyphenoxy)ethoxy>ethoxy>ethoxy>ethoxy>phenoxy>ethoxy>ethoxy>ethoxy>ethoxy>benzene

Base Information

Chemical Name:1,4-bis<2-<2-<2-<2-<<2-<2-<2-<2-(4-benzyloxyphenoxy)ethoxy>ethoxy>ethoxy>ethoxy>phenoxy>ethoxy>ethoxy>ethoxy>ethoxy>benzene
CAS No.:138611-00-4
Molecular Formula:C₇₆H₉₈O₂₂
Molecular Weight:1363.6
Hs Code.:

Synonyms:1,4-bis<2-<2-<2-<2-<<2-<2-<2-<2-(4-benzyloxyphenoxy)ethoxy>ethoxy>ethoxy>ethoxy>phenoxy>ethoxy>ethoxy>ethoxy>ethoxy>benzene

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Chemical Property of 1,4-bis<2-<2-<2-<2-<<2-<2-<2-<2-(4-benzyloxyphenoxy)ethoxy>ethoxy>ethoxy>ethoxy>phenoxy>ethoxy>ethoxy>ethoxy>ethoxy>benzene

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Technology Process of 1,4-bis<2-<2-<2-<2-<<2-<2-<2-<2-(4-benzyloxyphenoxy)ethoxy>ethoxy>ethoxy>ethoxy>phenoxy>ethoxy>ethoxy>ethoxy>ethoxy>benzene

There total 7 articles about 1,4-bis<2-<2-<2-<2-<<2-<2-<2-<2-(4-benzyloxyphenoxy)ethoxy>ethoxy>ethoxy>ethoxy>phenoxy>ethoxy>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:

: 103-16-2
4-Benzyloxyphenol

: 138611-00-4
1,4-bis<2-<2-<2-<2-<<2-<2-<2-<2-(4-benzyloxyphenoxy)ethoxy>ethoxy>ethoxy>ethoxy>phenoxy>ethoxy>ethoxy>ethoxy>ethoxy>benzene

Guidance literature:: Multi-step reaction with 6 steps

1: 1.) K₂CO₃ / 1.) DMF, 50 deg C, 2.) DMF, 75 deg C, 4 d

2: 78 percent / Et₃N / CH₂Cl₂ / 18 h / Ambient temperature

3: 1.) NaH / 1.) THF, from RT to 50 deg C, 1 h, 2.) THF, 75 deg C, 5 d

4: 90 percent / H₂ / 10percent Pd/C / CHCl₃; methanol / 24 h

5: 73 percent / K₂CO₃ / dimethylformamide / 7 h / 80 °C

6: 1.) NaH / 1.)THF, 50 deg C, 1 h, 2.) THF, 75 deg C_. 5 d

With hydrogen; sodium hydride; potassium carbonate; triethylamine; palladium on activated charcoal; In methanol; dichloromethane; chloroform; N,N-dimethyl-formamide;

Reference yield:

: 142879-00-3
1-<2-(2-hydroxyethoxy)ethoxy>-4-benzyloxybenzene

: 138611-00-4
1,4-bis<2-<2-<2-<2-<<2-<2-<2-<2-(4-benzyloxyphenoxy)ethoxy>ethoxy>ethoxy>ethoxy>phenoxy>ethoxy>ethoxy>ethoxy>ethoxy>benzene

Guidance literature:: Multi-step reaction with 5 steps

1: 78 percent / Et₃N / CH₂Cl₂ / 18 h / Ambient temperature

2: 1.) NaH / 1.) THF, from RT to 50 deg C, 1 h, 2.) THF, 75 deg C, 5 d

3: 90 percent / H₂ / 10percent Pd/C / CHCl₃; methanol / 24 h

4: 73 percent / K₂CO₃ / dimethylformamide / 7 h / 80 °C

5: 1.) NaH / 1.)THF, 50 deg C, 1 h, 2.) THF, 75 deg C_. 5 d

With hydrogen; sodium hydride; potassium carbonate; triethylamine; palladium on activated charcoal; In methanol; dichloromethane; chloroform; N,N-dimethyl-formamide;

Reference yield:

: 134881-64-4
1,4-bis<2-<2-<2-<2-(4-benzyloxyphenoxy)ethoxy>ethoxy>ethoxy>ethoxy>benzene

: 138611-00-4
1,4-bis<2-<2-<2-<2-<<2-<2-<2-<2-(4-benzyloxyphenoxy)ethoxy>ethoxy>ethoxy>ethoxy>phenoxy>ethoxy>ethoxy>ethoxy>ethoxy>benzene

Guidance literature:: Multi-step reaction with 3 steps

1: 90 percent / H₂ / 10percent Pd/C / CHCl₃; methanol / 24 h

2: 73 percent / K₂CO₃ / dimethylformamide / 7 h / 80 °C

3: 1.) NaH / 1.)THF, 50 deg C, 1 h, 2.) THF, 75 deg C_. 5 d

With hydrogen; sodium hydride; potassium carbonate; palladium on activated charcoal; In methanol; chloroform; N,N-dimethyl-formamide;