(E)-1,2-bis(methoxymethoxy)-4-(3-(methoxymethoxy)-5-(prop-2-ynyloxy)styryl)benzene

Base Information

Chemical Name:(E)-1,2-bis(methoxymethoxy)-4-(3-(methoxymethoxy)-5-(prop-2-ynyloxy)styryl)benzene
CAS No.:1392500-12-7
Molecular Formula:C₂₃H₂₆O₇
Molecular Weight:414.455
Hs Code.:

Synonyms:(E)-1,2-bis(methoxymethoxy)-4-(3-(methoxymethoxy)-5-(prop-2-ynyloxy)styryl)benzene

Suppliers and Price of (E)-1,2-bis(methoxymethoxy)-4-(3-(methoxymethoxy)-5-(prop-2-ynyloxy)styryl)benzene

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (E)-1,2-bis(methoxymethoxy)-4-(3-(methoxymethoxy)-5-(prop-2-ynyloxy)styryl)benzene

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (E)-1,2-bis(methoxymethoxy)-4-(3-(methoxymethoxy)-5-(prop-2-ynyloxy)styryl)benzene

There total 2 articles about (E)-1,2-bis(methoxymethoxy)-4-(3-(methoxymethoxy)-5-(prop-2-ynyloxy)styryl)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:

: 1392500-09-2
C₁₂H₁₄O₄

: 1392500-12-7
(E)-1,2-bis(methoxymethoxy)-4-(3-(methoxymethoxy)-5-(prop-2-ynyloxy)styryl)benzene

Guidance literature:: Multi-step reaction with 3 steps

1.1: 2,6-dimethylpyridine; carbon tetrabromide; triphenylphosphine / dichloromethane / 0.5 h / 0 °C / Inert atmosphere

2.1: 3 h / 100 °C / Inert atmosphere

3.1: sodium hydride / tetrahydrofuran; mineral oil / 0.17 h / 20 °C / Inert atmosphere

3.2: 3 h / 20 °C / Inert atmosphere

With 2,6-dimethylpyridine; carbon tetrabromide; sodium hydride; triphenylphosphine; In tetrahydrofuran; dichloromethane; mineral oil; 3.1: Horner-Wadsworth-Emmons Wittig olefination / 3.2: Horner-Wadsworth-Emmons Wittig olefination;
DOI:10.1016/j.bmcl.2012.06.019

Reference yield:

: 848474-32-8
3-methoxymethyloxy-5-hydroxybenzyl alcohol

: 1392500-12-7
(E)-1,2-bis(methoxymethoxy)-4-(3-(methoxymethoxy)-5-(prop-2-ynyloxy)styryl)benzene

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium carbonate / acetone / 4 h / Inert atmosphere; Reflux

2.1: 2,6-dimethylpyridine; carbon tetrabromide; triphenylphosphine / dichloromethane / 0.5 h / 0 °C / Inert atmosphere

3.1: 3 h / 100 °C / Inert atmosphere

4.1: sodium hydride / tetrahydrofuran; mineral oil / 0.17 h / 20 °C / Inert atmosphere

4.2: 3 h / 20 °C / Inert atmosphere

With 2,6-dimethylpyridine; carbon tetrabromide; sodium hydride; potassium carbonate; triphenylphosphine; In tetrahydrofuran; dichloromethane; acetone; mineral oil; 4.1: Horner-Wadsworth-Emmons Wittig olefination / 4.2: Horner-Wadsworth-Emmons Wittig olefination;
DOI:10.1016/j.bmcl.2012.06.019

Reference yield: 73.0%

: 1392500-07-0
5,5'-(2-azidopropane-1,3-diyl)bis(oxy)bis(2,2-dimethyl-1,3-dioxane)

: 1392500-12-7
(E)-1,2-bis(methoxymethoxy)-4-(3-(methoxymethoxy)-5-(prop-2-ynyloxy)styryl)benzene

: 1392500-13-8
(E)-1-(1,3-bis(2,2-dimethyl-1,3-dioxan-5-yloxy)propan-2-yl)-4-((3-(3,4-bis(methoxymethoxy)styryl)-5-(methoxymethoxy)phenoxy)methyl)-1H-1,2,3-triazole

Guidance literature:: With copper(ll) sulfate pentahydrate; sodium L-ascorbate; In water; tert-butyl alcohol; at 20 ℃; for 6h; Inert atmosphere;
DOI:10.1016/j.bmcl.2012.06.019