1-<2,4-bis(benzyloxy)phenyl>-3,3-dimethoxy-2-(2,3,4-trimethoxyphenyl)propane-1-one

Base Information

Chemical Name:1-<2,4-bis(benzyloxy)phenyl>-3,3-dimethoxy-2-(2,3,4-trimethoxyphenyl)propane-1-one
CAS No.:148356-31-4
Molecular Formula:C₃₄H₃₆O₈
Molecular Weight:572.655
Hs Code.:

Synonyms:1-<2,4-bis(benzyloxy)phenyl>-3,3-dimethoxy-2-(2,3,4-trimethoxyphenyl)propane-1-one

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Chemical Property of 1-<2,4-bis(benzyloxy)phenyl>-3,3-dimethoxy-2-(2,3,4-trimethoxyphenyl)propane-1-one

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Technology Process of 1-<2,4-bis(benzyloxy)phenyl>-3,3-dimethoxy-2-(2,3,4-trimethoxyphenyl)propane-1-one

There total 1 articles about 1-<2,4-bis(benzyloxy)phenyl>-3,3-dimethoxy-2-(2,3,4-trimethoxyphenyl)propane-1-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:

: 2103-57-3
2,3,4-trimethoxybenzaldehyde

: 148356-31-4
1-<2,4-bis(benzyloxy)phenyl>-3,3-dimethoxy-2-(2,3,4-trimethoxyphenyl)propane-1-one

Guidance literature:: Multi-step reaction with 2 steps

1: 82.5 percent / 50percent aq. KOH / ethanol / 24 h / Ambient temperature

2: thallium nitrate / CHCl₃ / Ambient temperature

With potassium hydroxide; thallium(I) nitrate; In ethanol; chloroform;

Reference yield: 70.5%

: 148356-31-4
1-<2,4-bis(benzyloxy)phenyl>-3,3-dimethoxy-2-(2,3,4-trimethoxyphenyl)propane-1-one

: 148356-32-5
1-(2,4-dihydroxyphenyl)-3,3-dimethoxy-2-(2,3,4-trimethoxyphenyl)propane-1-one

Guidance literature:: With hydrogen; triethylamine; palladium on activated charcoal; In ethyl acetate; under 760 Torr; Ambient temperature;

Reference yield:

: 148356-31-4
1-<2,4-bis(benzyloxy)phenyl>-3,3-dimethoxy-2-(2,3,4-trimethoxyphenyl)propane-1-one

: 2',3',4',7-tetrahydroxyisoflavone

Guidance literature:: Multi-step reaction with 3 steps

1: 70.5 percent / H₂, triethylamine / 10percent Pd/C / ethyl acetate / 760 Torr / Ambient temperature

2: 5percent HCl / methanol / 2 h / Heating

3: 63.6 percent / hydroiodic acid / 2 h / Heating

With hydrogenchloride; hydrogen iodide; hydrogen; triethylamine; palladium on activated charcoal; In methanol; ethyl acetate;