4-[(E)-2-[3,5-bis(benzyloxy)phenyl]vinyl]-1,2-bis[(methoxyethoxy)methoxy]benzene

Base Information

Chemical Name:4-[(E)-2-[3,5-bis(benzyloxy)phenyl]vinyl]-1,2-bis[(methoxyethoxy)methoxy]benzene
CAS No.:639806-48-7
Molecular Formula:C₃₆H₄₀O₈
Molecular Weight:600.709
Hs Code.:

Synonyms:4-[(E)-2-[3,5-bis(benzyloxy)phenyl]vinyl]-1,2-bis[(methoxyethoxy)methoxy]benzene

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Chemical Property of 4-[(E)-2-[3,5-bis(benzyloxy)phenyl]vinyl]-1,2-bis[(methoxyethoxy)methoxy]benzene

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Technology Process of 4-[(E)-2-[3,5-bis(benzyloxy)phenyl]vinyl]-1,2-bis[(methoxyethoxy)methoxy]benzene

There total 1 articles about 4-[(E)-2-[3,5-bis(benzyloxy)phenyl]vinyl]-1,2-bis[(methoxyethoxy)methoxy]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: 81.0%

: 99815-24-4
3,4-bis-[(methoxyethoxy)-methoxy]-benzaldehyde

: (3,5-bis-benzyloxy-benzyl)-triphenyl-phosphonium; chloride

: 639806-48-7
4-[(E)-2-[3,5-bis(benzyloxy)phenyl]vinyl]-1,2-bis[(methoxyethoxy)methoxy]benzene

Guidance literature:: (3,5-bis-benzyloxy-benzyl)-triphenyl-phosphonium; chloride; With n-butyllithium; In tetrahydrofuran; at 20 ℃; for 0.5h;

3,4-bis-[(methoxyethoxy)-methoxy]-benzaldehyde; In tetrahydrofuran; at 20 ℃; for 3h;

Reference yield: 85.0%

: 639806-48-7
4-[(E)-2-[3,5-bis(benzyloxy)phenyl]vinyl]-1,2-bis[(methoxyethoxy)methoxy]benzene

: 639806-49-8
4-[(E)-2-[3,5-bis(benzyloxy)phenyl]vinyl]-1,2-dihydroxybenzene

Guidance literature:: With trifluoroacetic acid; In chloroform; at 20 ℃; for 3h;

Reference yield:

: 639806-48-7
4-[(E)-2-[3,5-bis(benzyloxy)phenyl]vinyl]-1,2-bis[(methoxyethoxy)methoxy]benzene

: Maackin

Guidance literature:: Multi-step reaction with 3 steps

1.1: 85 percent / trifluoroacetic acid / CHCl₃ / 3 h / 20 °C

2.1: silver oxide / benzene; acetone / 7 h / 55 - 60 °C

2.2: 46 percent / K₂CO₃ / dimethylformamide / 12 h / 20 °C

3.1: 72 percent / t-BuNH₂; t-BuOH; potassium / 18-crown-6 / tetrahydrofuran / 3 h

With potassium; tert-butylamine; trifluoroacetic acid; silver(l) oxide; tert-butyl alcohol; 18-crown-6 ether; In tetrahydrofuran; chloroform; acetone; benzene;