2-(2,4-dimethoxyphenyl)-5-hydroxy-7-methoxy-3-(3-methylbut-2-en-1-yl)-6-(3-methylbutanoyl)-4H-chromen-4-one

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Chemical Name:2-(2,4-dimethoxyphenyl)-5-hydroxy-7-methoxy-3-(3-methylbut-2-en-1-yl)-6-(3-methylbutanoyl)-4H-chromen-4-one
CAS No.:1443276-24-1
Molecular Formula:C₂₈H₃₂O₇
Molecular Weight:480.558
Hs Code.:

Synonyms:2-(2,4-dimethoxyphenyl)-5-hydroxy-7-methoxy-3-(3-methylbut-2-en-1-yl)-6-(3-methylbutanoyl)-4H-chromen-4-one

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Chemical Property of 2-(2,4-dimethoxyphenyl)-5-hydroxy-7-methoxy-3-(3-methylbut-2-en-1-yl)-6-(3-methylbutanoyl)-4H-chromen-4-one

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Technology Process of 2-(2,4-dimethoxyphenyl)-5-hydroxy-7-methoxy-3-(3-methylbut-2-en-1-yl)-6-(3-methylbutanoyl)-4H-chromen-4-one

There total 6 articles about 2-(2,4-dimethoxyphenyl)-5-hydroxy-7-methoxy-3-(3-methylbut-2-en-1-yl)-6-(3-methylbutanoyl)-4H-chromen-4-one 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: 74.0%

: 1443276-21-8
1-(2,6-dihydroxy-4-methoxy-3-(3-methylbutanoyl)phenyl)-3-(2,4-dimethoxyphenyl)-2-(3-methylbut-2-en-1-yl)propane-1,3-dione

: 1443276-24-1
2-(2,4-dimethoxyphenyl)-5-hydroxy-7-methoxy-3-(3-methylbut-2-en-1-yl)-6-(3-methylbutanoyl)-4H-chromen-4-one

Guidance literature:: With sulfuric acid; In acetic acid; at 20 ℃; for 0.5h; regioselective reaction;
DOI:10.1016/j.tet.2013.05.024

Reference yield:

: 832-58-6
1-(2,4,6-trimethoxyphenyl)ethanone

: 1443276-24-1
2-(2,4-dimethoxyphenyl)-5-hydroxy-7-methoxy-3-(3-methylbut-2-en-1-yl)-6-(3-methylbutanoyl)-4H-chromen-4-one

Guidance literature:: Multi-step reaction with 5 steps

1.1: aluminum (III) chloride / dichloromethane / 24 h / 0 °C / Reflux

2.1: sodium hydride / tetrahydrofuran / 0.25 h / 0 °C

2.2: 0.5 h / Reflux

3.1: sodium hydride / tetrahydrofuran / 1.67 h / 0 °C / Reflux

4.1: potassium carbonate / acetone / 0.5 h

4.2: 24 h / Reflux

5.1: sulfuric acid / acetic acid / 0.5 h / 20 °C

With aluminum (III) chloride; sulfuric acid; sodium hydride; potassium carbonate; In tetrahydrofuran; dichloromethane; acetic acid; acetone; 3.1: |Baker-Venkataraman Rearrangement;
DOI:10.1016/j.tet.2013.05.024

Reference yield:

: 1443276-18-3
1-(3-acetyl-2-hydroxy-4,6-dimethoxyphenyl)-3-methyl-1-butanone

: 1443276-24-1
2-(2,4-dimethoxyphenyl)-5-hydroxy-7-methoxy-3-(3-methylbut-2-en-1-yl)-6-(3-methylbutanoyl)-4H-chromen-4-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydride / tetrahydrofuran / 0.25 h / 0 °C

1.2: 0.5 h / Reflux

2.1: sodium hydride / tetrahydrofuran / 1.67 h / 0 °C / Reflux

3.1: potassium carbonate / acetone / 0.5 h

3.2: 24 h / Reflux

4.1: sulfuric acid / acetic acid / 0.5 h / 20 °C

With sulfuric acid; sodium hydride; potassium carbonate; In tetrahydrofuran; acetic acid; acetone; 2.1: |Baker-Venkataraman Rearrangement;
DOI:10.1016/j.tet.2013.05.024