2-(3,4-Bis-benzyloxy-phenyl)-5,7-dimethoxy-6-(3-methyl-butoxy)-chromen-4-one

Base Information

Chemical Name:2-(3,4-Bis-benzyloxy-phenyl)-5,7-dimethoxy-6-(3-methyl-butoxy)-chromen-4-one
CAS No.:103777-11-3
Molecular Formula:C₃₆H₃₆O₇
Molecular Weight:580.678
Hs Code.:

Synonyms:2-(3,4-Bis-benzyloxy-phenyl)-5,7-dimethoxy-6-(3-methyl-butoxy)-chromen-4-one

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Chemical Property of 2-(3,4-Bis-benzyloxy-phenyl)-5,7-dimethoxy-6-(3-methyl-butoxy)-chromen-4-one

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Technology Process of 2-(3,4-Bis-benzyloxy-phenyl)-5,7-dimethoxy-6-(3-methyl-butoxy)-chromen-4-one

There total 1 articles about 2-(3,4-Bis-benzyloxy-phenyl)-5,7-dimethoxy-6-(3-methyl-butoxy)-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: 88.0%

: 27181-96-0
3',4'-bis(benzyloxy)-6-hydroxy-5,7-dimethoxyflavone

: 541-28-6
isopentyl iodide

: 103777-11-3
2-(3,4-Bis-benzyloxy-phenyl)-5,7-dimethoxy-6-(3-methyl-butoxy)-chromen-4-one

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; acetone; for 8h; Heating;
DOI:10.1021/jm00161a021

Reference yield: 90.0%

: 103777-11-3
2-(3,4-Bis-benzyloxy-phenyl)-5,7-dimethoxy-6-(3-methyl-butoxy)-chromen-4-one

: 103776-60-9
2-(3,4-Dihydroxy-phenyl)-5,7-dimethoxy-6-(3-methyl-butoxy)-chromen-4-one

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; ethyl acetate;
DOI:10.1021/jm00161a021

Reference yield:

: 103777-11-3
2-(3,4-Bis-benzyloxy-phenyl)-5,7-dimethoxy-6-(3-methyl-butoxy)-chromen-4-one

: 103776-91-6
2-(3,4-Dihydroxy-phenyl)-5-hydroxy-7-methoxy-6-(3-methyl-butoxy)-chromen-4-one

Guidance literature:: Multi-step reaction with 4 steps

1: 90 percent / H₂ / 10percent Pd/C / methanol; ethyl acetate

2: pyridine / Heating

3: AlCl₃ / acetonitrile / 1.5 h / 60 °C

4: 6 M HCl / methanol / 4 h / Heating

With pyridine; hydrogenchloride; aluminium trichloride; hydrogen; palladium on activated charcoal; In methanol; ethyl acetate; acetonitrile;
DOI:10.1021/jm00161a021