3-(1-Benzyl-3-chlorooxalyl-2-methyl-1H-indol-4-yl)-propionic acid methyl ester

Base Information

Chemical Name:3-(1-Benzyl-3-chlorooxalyl-2-methyl-1H-indol-4-yl)-propionic acid methyl ester
CAS No.:1026029-76-4
Molecular Formula:C₂₂H₂₀ClNO₄
Molecular Weight:397.858
Hs Code.:

Synonyms:3-(1-Benzyl-3-chlorooxalyl-2-methyl-1H-indol-4-yl)-propionic acid methyl ester

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Chemical Property of 3-(1-Benzyl-3-chlorooxalyl-2-methyl-1H-indol-4-yl)-propionic acid methyl ester

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Technology Process of 3-(1-Benzyl-3-chlorooxalyl-2-methyl-1H-indol-4-yl)-propionic acid methyl ester

There total 6 articles about 3-(1-Benzyl-3-chlorooxalyl-2-methyl-1H-indol-4-yl)-propionic 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:

: 100-39-0
benzyl bromide

: 1026029-76-4
3-(1-Benzyl-3-chlorooxalyl-2-methyl-1H-indol-4-yl)-propionic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 1.) H₂SO₄, AgSO₄, 2.) Br₂, 3.) K₂CO₃, 4.) n-BuLi

2: 69 percent / tetrahydrofuran / 19 h / Heating

3: 69 percent / dichlorodicyanoquinone / dioxane / 0.25 h / 85 °C

4: H₂ / 10percent Pd/C / tetrahydrofuran; methanol / 2.5 h / 760 Torr

5: CH₂Cl₂ / 1 h

With n-butyllithium; silver(II) sulfate; sulfuric acid; hydrogen; bromine; potassium carbonate; 2,3-dicyano-5,6-dichloro-p-benzoquinone; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane;
DOI:10.1021/jm960487f

Reference yield:

: 185299-02-9
1-Benzyl-2-methyl-2,3-dihydro-1H-indole-4-carbaldehyde

: 1026029-76-4
3-(1-Benzyl-3-chlorooxalyl-2-methyl-1H-indol-4-yl)-propionic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 69 percent / tetrahydrofuran / 19 h / Heating

2: 69 percent / dichlorodicyanoquinone / dioxane / 0.25 h / 85 °C

3: H₂ / 10percent Pd/C / tetrahydrofuran; methanol / 2.5 h / 760 Torr

4: CH₂Cl₂ / 1 h

With hydrogen; 2,3-dicyano-5,6-dichloro-p-benzoquinone; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane;
DOI:10.1021/jm960487f

Reference yield:

: (E)-3-(1-Benzyl-2-methyl-1H-indol-4-yl)-acrylic acid methyl ester

: 1026029-76-4
3-(1-Benzyl-3-chlorooxalyl-2-methyl-1H-indol-4-yl)-propionic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: H₂ / 10percent Pd/C / tetrahydrofuran; methanol / 2.5 h / 760 Torr

2: CH₂Cl₂ / 1 h

With hydrogen; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/jm960487f