(E,E)-1,4-bis[3'-hydroxy-4'-(methanesulfonyloxy)styryl]benzene

Base Information

Chemical Name:(E,E)-1,4-bis[3'-hydroxy-4'-(methanesulfonyloxy)styryl]benzene
CAS No.:491853-79-3
Molecular Formula:C₂₄H₂₂O₈S₂
Molecular Weight:502.566
Hs Code.:

Synonyms:(E,E)-1,4-bis[3'-hydroxy-4'-(methanesulfonyloxy)styryl]benzene

Suppliers and Price of (E,E)-1,4-bis[3'-hydroxy-4'-(methanesulfonyloxy)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,E)-1,4-bis[3'-hydroxy-4'-(methanesulfonyloxy)styryl]benzene

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (E,E)-1,4-bis[3'-hydroxy-4'-(methanesulfonyloxy)styryl]benzene

There total 5 articles about (E,E)-1,4-bis[3'-hydroxy-4'-(methanesulfonyloxy)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: 83.0%

: 491853-78-2
(E,E)-1,4-bis[3'-methoxymethoxy-4'-(methanesulfonyloxy)styryl]benzene

: 491853-79-3
(E,E)-1,4-bis[3'-hydroxy-4'-(methanesulfonyloxy)styryl]benzene

Guidance literature:: With water; acetic acid; at 110 ℃; for 1.41667h;
DOI:10.1002/jlcr.585

Reference yield:

: 621-59-0
isovanillin

: 491853-79-3
(E,E)-1,4-bis[3'-hydroxy-4'-(methanesulfonyloxy)styryl]benzene

Guidance literature:: Multi-step reaction with 5 steps

1: 16 percent / p-toluenesulfonic acid; 3 Angstroem molecular sieves / CH₂Cl₂ / Heating

2: 83 percent / sodium methoxide / dimethylsulfoxide; methanol / 20 °C

3: 63 percent / potassium tert-butoxide; sodium thioethoxide / dimethylformamide / 2.33 h / Heating

4: 83 percent / triethylamine / CH₂Cl₂ / 22 h / 20 °C

5: 83 percent / glacial acetic acid; water / 1.42 h / 110 °C

With 3 A molecular sieve; sodium thioethoxide; potassium tert-butylate; water; sodium methylate; toluene-4-sulfonic acid; acetic acid; triethylamine; In methanol; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide; 2: Wittig-Horner reaction;
DOI:10.1002/jlcr.585

Reference yield:

: 5779-98-6
O-methoxymethylisovanillin

: 491853-79-3
(E,E)-1,4-bis[3'-hydroxy-4'-(methanesulfonyloxy)styryl]benzene

Guidance literature:: Multi-step reaction with 4 steps

1: 83 percent / sodium methoxide / dimethylsulfoxide; methanol / 20 °C

2: 63 percent / potassium tert-butoxide; sodium thioethoxide / dimethylformamide / 2.33 h / Heating

3: 83 percent / triethylamine / CH₂Cl₂ / 22 h / 20 °C

4: 83 percent / glacial acetic acid; water / 1.42 h / 110 °C

With sodium thioethoxide; potassium tert-butylate; water; sodium methylate; acetic acid; triethylamine; In methanol; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide; 1: Wittig-Horner reaction;
DOI:10.1002/jlcr.585