(E)-ethyl-2-(2-methoxy-4-(3-oxo-3-(3,4,5-trimethoxyphenyl)prop-1-en-1-yl)phenoxy)acetate

Base Information

Chemical Name:(E)-ethyl-2-(2-methoxy-4-(3-oxo-3-(3,4,5-trimethoxyphenyl)prop-1-en-1-yl)phenoxy)acetate
CAS No.:1357099-32-1
Molecular Formula:C₂₃H₂₆O₈
Molecular Weight:430.455
Hs Code.:

Synonyms:(E)-ethyl-2-(2-methoxy-4-(3-oxo-3-(3,4,5-trimethoxyphenyl)prop-1-en-1-yl)phenoxy)acetate

Suppliers and Price of (E)-ethyl-2-(2-methoxy-4-(3-oxo-3-(3,4,5-trimethoxyphenyl)prop-1-en-1-yl)phenoxy)acetate

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

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Chemical Property of (E)-ethyl-2-(2-methoxy-4-(3-oxo-3-(3,4,5-trimethoxyphenyl)prop-1-en-1-yl)phenoxy)acetate

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Technology Process of (E)-ethyl-2-(2-methoxy-4-(3-oxo-3-(3,4,5-trimethoxyphenyl)prop-1-en-1-yl)phenoxy)acetate

There total 3 articles about (E)-ethyl-2-(2-methoxy-4-(3-oxo-3-(3,4,5-trimethoxyphenyl)prop-1-en-1-yl)phenoxy)acetate 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: 76.0%

: 1202275-67-9
(E)-3-(4''-hydroxy-3-methoxyphenyl)-1-(3',4',5'-trimethoxyphenyl)-2-propen-1-one

: 105-36-2
ethyl bromoacetate

: 1357099-32-1
(E)-ethyl-2-(2-methoxy-4-(3-oxo-3-(3,4,5-trimethoxyphenyl)prop-1-en-1-yl)phenoxy)acetate

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 14h;
DOI:10.1016/j.ejmech.2011.11.024

Reference yield:

: 1136-86-3
methyl (3,4,5-trimethoxyphenyl) ketone

: 1357099-32-1
(E)-ethyl-2-(2-methoxy-4-(3-oxo-3-(3,4,5-trimethoxyphenyl)prop-1-en-1-yl)phenoxy)acetate

Guidance literature:: Multi-step reaction with 2 steps

1: potassium hydroxide / ethanol; water / 6 h / 20 °C

2: potassium carbonate / N,N-dimethyl-formamide / 14 h / 20 °C

With potassium carbonate; potassium hydroxide; In ethanol; water; N,N-dimethyl-formamide; 1: Claisen-Schmidt condensation;
DOI:10.1016/j.ejmech.2011.11.024

Reference yield:

: 121-33-5,8014-42-4
vanillin

: 1357099-32-1
(E)-ethyl-2-(2-methoxy-4-(3-oxo-3-(3,4,5-trimethoxyphenyl)prop-1-en-1-yl)phenoxy)acetate

Guidance literature:: Multi-step reaction with 2 steps

1: potassium hydroxide / ethanol; water / 6 h / 20 °C

2: potassium carbonate / N,N-dimethyl-formamide / 14 h / 20 °C

With potassium carbonate; potassium hydroxide; In ethanol; water; N,N-dimethyl-formamide; 1: Claisen-Schmidt condensation;
DOI:10.1016/j.ejmech.2011.11.024