(Z)-3-(3,4-Dimethoxy-phenyl)-3-(2-phenylsulfanyl-ethylamino)-acrylic acid methyl ester

Base Information

Chemical Name:(Z)-3-(3,4-Dimethoxy-phenyl)-3-(2-phenylsulfanyl-ethylamino)-acrylic acid methyl ester
CAS No.:212050-49-2
Molecular Formula:C₂₀H₂₃NO₄S
Molecular Weight:373.473
Hs Code.:

Synonyms:(Z)-3-(3,4-Dimethoxy-phenyl)-3-(2-phenylsulfanyl-ethylamino)-acrylic acid methyl ester

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Chemical Property of (Z)-3-(3,4-Dimethoxy-phenyl)-3-(2-phenylsulfanyl-ethylamino)-acrylic acid methyl ester

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Technology Process of (Z)-3-(3,4-Dimethoxy-phenyl)-3-(2-phenylsulfanyl-ethylamino)-acrylic acid methyl ester

There total 3 articles about (Z)-3-(3,4-Dimethoxy-phenyl)-3-(2-phenylsulfanyl-ethylamino)-acrylic acid methyl 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: 90.0%

: 2014-75-7
2-(phenylthio)ethanamine

: 74053-93-3
methyl 3-(3,4-dimethoxyphenyl)-3-oxopropionate

: 212050-49-2
(Z)-3-(3,4-Dimethoxy-phenyl)-3-(2-phenylsulfanyl-ethylamino)-acrylic acid methyl ester

Guidance literature:: With acetic acid; In methanol; for 27h; Heating;
DOI:10.1248/cpb.46.906

Reference yield:

: 3111-52-2
potassium thiophenolate

: 212050-49-2
(Z)-3-(3,4-Dimethoxy-phenyl)-3-(2-phenylsulfanyl-ethylamino)-acrylic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: ethanol / 1.5 h / Heating

2: 90 percent / AcOH / methanol / 27 h / Heating

With acetic acid; In methanol; ethanol;
DOI:10.1248/cpb.46.906

Reference yield:

: 3535-37-3
3,4-dimethoxybenzoic acid chloride

: 212050-49-2
(Z)-3-(3,4-Dimethoxy-phenyl)-3-(2-phenylsulfanyl-ethylamino)-acrylic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 2.) NH₄Cl, 28percent aq. NH₄OH / 1.) ether, reflux, 3 h, 2.) 100 deg C

2: 90 percent / AcOH / methanol / 27 h / Heating

With ammonium hydroxide; ammonium chloride; acetic acid; In methanol;
DOI:10.1248/cpb.46.906