5-benzoyloxy-3'-hydroxy-3,4'-dimethoxydihydrostilbene

Base Information

Chemical Name:5-benzoyloxy-3'-hydroxy-3,4'-dimethoxydihydrostilbene
CAS No.:76735-49-4
Molecular Formula:C₂₃H₂₂O₅
Molecular Weight:378.425
Hs Code.:

Synonyms:5-benzoyloxy-3'-hydroxy-3,4'-dimethoxydihydrostilbene

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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 5-benzoyloxy-3'-hydroxy-3,4'-dimethoxydihydrostilbene

Chemical Property:

Purity/Quality:

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Hazard Codes:

MSDS Files:: SDS file from LookChem

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Technology Process of 5-benzoyloxy-3'-hydroxy-3,4'-dimethoxydihydrostilbene

There total 11 articles about 5-benzoyloxy-3'-hydroxy-3,4'-dimethoxydihydrostilbene 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: 97.0%

: 76735-47-2
Benzoic acid 3-[(E)-2-(3-benzyloxy-4-methoxy-phenyl)-vinyl]-5-methoxy-phenyl ester

: 76735-49-4
5-benzoyloxy-3'-hydroxy-3,4'-dimethoxydihydrostilbene

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethyl acetate; at 20 ℃; for 16h;

Reference yield:

: 76735-46-1,76735-60-9
3'-benzyloxy-5-hydroxy-3,4'-dimethoxystilbene

: 76735-49-4
5-benzoyloxy-3'-hydroxy-3,4'-dimethoxydihydrostilbene

Guidance literature:: Multi-step reaction with 2 steps

1: 71 percent / pyridine / 22 h

2: 97 percent / H₂ / 10percent palladium on carbon / ethyl acetate / 16 h / 20 °C

With pyridine; hydrogen; palladium on activated charcoal; In ethyl acetate;

Reference yield:

: 6346-05-0
3-benzyloxy-4-methoxybenzaldehyde

: 76735-49-4
5-benzoyloxy-3'-hydroxy-3,4'-dimethoxydihydrostilbene

Guidance literature:: Multi-step reaction with 3 steps

1: 73 percent / 1.) n-butyl-lithium / tetrahydrofuran; hexane / 1.) 20 deg C, 90 min, 2.) 20 deg C, 18 h

2: 71 percent / pyridine / 22 h

3: 97 percent / H₂ / 10percent palladium on carbon / ethyl acetate / 16 h / 20 °C

With pyridine; n-butyllithium; hydrogen; palladium on activated charcoal; In tetrahydrofuran; hexane; ethyl acetate;