(+)-(3aR,4S,5S,7aR)-2-(2,4-dimethoxybenzyl)-3a,5-dimethyl-1-oxo-2,3,3a,4,5,7a-hexahydro-1H-isoindole-4-carbaldehyde

Base Information

Chemical Name:(+)-(3aR,4S,5S,7aR)-2-(2,4-dimethoxybenzyl)-3a,5-dimethyl-1-oxo-2,3,3a,4,5,7a-hexahydro-1H-isoindole-4-carbaldehyde
CAS No.:1314240-59-9
Molecular Formula:C₂₀H₂₅NO₄
Molecular Weight:343.423
Hs Code.:

Synonyms:(+)-(3aR,4S,5S,7aR)-2-(2,4-dimethoxybenzyl)-3a,5-dimethyl-1-oxo-2,3,3a,4,5,7a-hexahydro-1H-isoindole-4-carbaldehyde

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Chemical Property of (+)-(3aR,4S,5S,7aR)-2-(2,4-dimethoxybenzyl)-3a,5-dimethyl-1-oxo-2,3,3a,4,5,7a-hexahydro-1H-isoindole-4-carbaldehyde

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Technology Process of (+)-(3aR,4S,5S,7aR)-2-(2,4-dimethoxybenzyl)-3a,5-dimethyl-1-oxo-2,3,3a,4,5,7a-hexahydro-1H-isoindole-4-carbaldehyde

There total 3 articles about (+)-(3aR,4S,5S,7aR)-2-(2,4-dimethoxybenzyl)-3a,5-dimethyl-1-oxo-2,3,3a,4,5,7a-hexahydro-1H-isoindole-4-carbaldehyde 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: 67.0%

: 1314240-57-7
(2E,4E)-N-(2,4-dimethoxybenzyl)-N-((E)-2-methyl-4-oxobut-2-enyl)hexa-2,4-dienamide

: 1314240-59-9
(+)-(3aR,4S,5S,7aR)-2-(2,4-dimethoxybenzyl)-3a,5-dimethyl-1-oxo-2,3,3a,4,5,7a-hexahydro-1H-isoindole-4-carbaldehyde

Guidance literature:: With C₁₄H₂₀N₂O₂*ClHO₄; In acetonitrile; at 3 ℃; for 54h;
DOI:10.1021/ol201461n

Reference yield:

: 1314240-55-5
(E)-4-((2E,4E)-N-(2,4-dimethoxybenzyl)-hexa-2,4-dienamido)-3-methylbut-2-enyl acetate

: 1314240-59-9
(+)-(3aR,4S,5S,7aR)-2-(2,4-dimethoxybenzyl)-3a,5-dimethyl-1-oxo-2,3,3a,4,5,7a-hexahydro-1H-isoindole-4-carbaldehyde

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate / methanol / 0.5 h / 20 °C

2: dichloromethane / 0.5 h / 23 °C

3: C₁₄H₂₀N₂O₂*ClHO₄ / acetonitrile / 54 h / 3 °C

With C₁₄H₂₀N₂O₂*ClHO₄; potassium carbonate; In methanol; dichloromethane; acetonitrile;
DOI:10.1021/ol201461n

Reference yield:

: 1314240-56-6
(2E,4E)-N-(2,4-dimethoxybenzyl)-N-((E)-4-hydroxy-2-methylbut-2-enyl)hexa-2,4-dienamide

: 1314240-59-9
(+)-(3aR,4S,5S,7aR)-2-(2,4-dimethoxybenzyl)-3a,5-dimethyl-1-oxo-2,3,3a,4,5,7a-hexahydro-1H-isoindole-4-carbaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1: dichloromethane / 0.5 h / 23 °C

2: C₁₄H₂₀N₂O₂*ClHO₄ / acetonitrile / 54 h / 3 °C

With C₁₄H₂₀N₂O₂*ClHO₄; In dichloromethane; acetonitrile;
DOI:10.1021/ol201461n