1,3-Benzenedicarboxylic acid, 5,5'-[1,2-ethanediylbis(oxy)]bis-, tetraethyl ester

Base Information

Chemical Name:1,3-Benzenedicarboxylic acid, 5,5'-[1,2-ethanediylbis(oxy)]bis-, tetraethyl ester
CAS No.:113585-29-8
Molecular Formula:C26H30O10
Molecular Weight:502.518
Hs Code.:

Synonyms:

Suppliers and Price of 1,3-Benzenedicarboxylic acid, 5,5'-[1,2-ethanediylbis(oxy)]bis-, tetraethyl ester

Supply Marketing:

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

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Total 1 raw suppliers

Chemical Property of 1,3-Benzenedicarboxylic acid, 5,5'-[1,2-ethanediylbis(oxy)]bis-, tetraethyl ester

Chemical Property:

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 1,3-Benzenedicarboxylic acid, 5,5'-[1,2-ethanediylbis(oxy)]bis-, tetraethyl ester

There total 2 articles about 1,3-Benzenedicarboxylic acid, 5,5'-[1,2-ethanediylbis(oxy)]bis-, tetraethyl ester 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: 64.0%

: 39630-68-7
diethyl 5-hydroxyisophthalate

: 106-93-4
ethylene dibromide

: 113585-29-8
1,2-bis( 3,5-dicarbethoxyphenoxy)ethane

Guidance literature:: With potassium carbonate; In acetone; at 60 ℃; for 24h;
DOI:10.1039/c0ce00474j

Reference yield:

: 618-83-7
5-Hydroxyisophthalic acid

: 113585-29-8
1,2-bis( 3,5-dicarbethoxyphenoxy)ethane

Guidance literature:: Multi-step reaction with 2 steps

1: 95 percent / HCl / 2 h

2: 57 percent / K₂CO₃ / dimethylformamide / 12 h / 60 °C

With hydrogenchloride; potassium carbonate; In N,N-dimethyl-formamide;
DOI:10.1021/ja00219a023