(R)-1-(allyloxy)-3-(3,4-bis(benzyloxy)phenyl)-1-oxopropan-2-yl (E)-3-(4-hydroxy-3-methoxyphenyl)acrylate

Base Information

Chemical Name:(R)-1-(allyloxy)-3-(3,4-bis(benzyloxy)phenyl)-1-oxopropan-2-yl (E)-3-(4-hydroxy-3-methoxyphenyl)acrylate
CAS No.:1510460-32-8
Molecular Formula:C₃₆H₃₄O₈
Molecular Weight:594.661
Hs Code.:

Synonyms:(R)-1-(allyloxy)-3-(3,4-bis(benzyloxy)phenyl)-1-oxopropan-2-yl (E)-3-(4-hydroxy-3-methoxyphenyl)acrylate

Suppliers and Price of (R)-1-(allyloxy)-3-(3,4-bis(benzyloxy)phenyl)-1-oxopropan-2-yl (E)-3-(4-hydroxy-3-methoxyphenyl)acrylate

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 (R)-1-(allyloxy)-3-(3,4-bis(benzyloxy)phenyl)-1-oxopropan-2-yl (E)-3-(4-hydroxy-3-methoxyphenyl)acrylate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (R)-1-(allyloxy)-3-(3,4-bis(benzyloxy)phenyl)-1-oxopropan-2-yl (E)-3-(4-hydroxy-3-methoxyphenyl)acrylate

There total 1 articles about (R)-1-(allyloxy)-3-(3,4-bis(benzyloxy)phenyl)-1-oxopropan-2-yl (E)-3-(4-hydroxy-3-methoxyphenyl)acrylate 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:

: 99353-00-1
rosmarinic acid methyl ester

: 1510460-32-8
(R)-1-(allyloxy)-3-(3,4-bis(benzyloxy)phenyl)-1-oxopropan-2-yl (E)-3-(4-hydroxy-3-methoxyphenyl)acrylate

Guidance literature:: Multi-step reaction with 6 steps

1: potassium carbonate / N,N-dimethyl-formamide / 16 h / 25 - 55 °C / Inert atmosphere

2: methanol; N,N-dimethyl-formamide / 4.5 h / 25 °C / Inert atmosphere

3: lithium hydroxide / methanol; tetrahydrofuran; water / 6 h / 0 - 45 °C / Inert atmosphere

4: potassium carbonate / N,N-dimethyl-formamide / 2 h / 25 °C / Inert atmosphere

5: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 3 h / 25 °C / Inert atmosphere

6: tetrabutyl ammonium fluoride; acetic acid / tetrahydrofuran / 1 h / 0 °C / Inert atmosphere

With dmap; tetrabutyl ammonium fluoride; potassium carbonate; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; lithium hydroxide; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1021/jo4023167