(Z)-methyl 3-(2,4-dimethoxyphenyl)-3-((2-ethoxy-2-oxoethyl)amino)acrylate

Base Information

Chemical Name:(Z)-methyl 3-(2,4-dimethoxyphenyl)-3-((2-ethoxy-2-oxoethyl)amino)acrylate
CAS No.:1435472-90-4
Molecular Formula:C₁₆H₂₁NO₆
Molecular Weight:323.346
Hs Code.:

Synonyms:(Z)-methyl 3-(2,4-dimethoxyphenyl)-3-((2-ethoxy-2-oxoethyl)amino)acrylate

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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 (Z)-methyl 3-(2,4-dimethoxyphenyl)-3-((2-ethoxy-2-oxoethyl)amino)acrylate

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Technology Process of (Z)-methyl 3-(2,4-dimethoxyphenyl)-3-((2-ethoxy-2-oxoethyl)amino)acrylate

There total 3 articles about (Z)-methyl 3-(2,4-dimethoxyphenyl)-3-((2-ethoxy-2-oxoethyl)amino)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: 69.0%

: 5680-79-5,883886-67-7
glycine ethyl ester hydrochloride

: 676348-64-4
methyl 3-(2,4-dimethoxyphenyl)-3-oxopropanoate

: 1435472-90-4
(Z)-methyl 3-(2,4-dimethoxyphenyl)-3-((2-ethoxy-2-oxoethyl)amino)acrylate

Guidance literature:: With acetic acid; triethylamine; In ethanol; at 100 ℃; for 18h;

Reference yield: 69.0%

: 623-33-6
glycine ethyl ester hydrochloride

: 676348-64-4
methyl 3-(2,4-dimethoxyphenyl)-3-oxopropanoate

: 1435472-90-4
(Z)-methyl 3-(2,4-dimethoxyphenyl)-3-((2-ethoxy-2-oxoethyl)amino)acrylate

Guidance literature:: With acetic acid; triethylamine; In ethanol; at 100 ℃; for 18h;
DOI:10.1021/acs.jmedchem.5b00963

Reference yield:

: 829-20-9
2',4'-dimethoxyacetophenone

: 1435472-90-4
(Z)-methyl 3-(2,4-dimethoxyphenyl)-3-((2-ethoxy-2-oxoethyl)amino)acrylate

Guidance literature:: Multi-step reaction with 2 steps

1: potassium tert-butylate / tetrahydrofuran; tert-butyl methyl ether / 20 °C / Inert atmosphere

2: triethylamine; acetic acid / ethanol / 18 h / 100 °C

With potassium tert-butylate; acetic acid; triethylamine; In tetrahydrofuran; ethanol; tert-butyl methyl ether;