2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-((2-nitrobenzyl)oxy)-4H-chromen-4-one

Base Information

Chemical Name:2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-((2-nitrobenzyl)oxy)-4H-chromen-4-one
CAS No.:1394914-31-8
Molecular Formula:C₂₂H₁₅NO₉
Molecular Weight:437.362
Hs Code.:

Synonyms:2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-((2-nitrobenzyl)oxy)-4H-chromen-4-one

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Chemical Property of 2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-((2-nitrobenzyl)oxy)-4H-chromen-4-one

Chemical Property:

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Technology Process of 2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-((2-nitrobenzyl)oxy)-4H-chromen-4-one

There total 4 articles about 2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-((2-nitrobenzyl)oxy)-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:

: C₃₀H₂₃NO₁₃

: 1394914-31-8
2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-((2-nitrobenzyl)oxy)-4H-chromen-4-one

Guidance literature:: With methanol; ammonia; at 0 ℃; for 1h;
DOI:10.1007/s12272-012-0108-9

Reference yield:

: 117-39-5,74893-81-5
quercetol

: 1394914-31-8
2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-((2-nitrobenzyl)oxy)-4H-chromen-4-one

Guidance literature:: Multi-step reaction with 4 steps

1: pyridine / 4 h / 80 °C

2: 1H-imidazole; thiophenol / 1-methyl-pyrrolidin-2-one / 0 - 20 °C

3: potassium carbonate / acetone / 20 °C

4: methanol; ammonia / 1 h / 0 °C

With pyridine; 1H-imidazole; methanol; ammonia; potassium carbonate; thiophenol; In 1-methyl-pyrrolidin-2-one; acetone;
DOI:10.1007/s12272-012-0108-9

Reference yield:

: 1064-06-8
3,5,7-triacetoxy-2-(3,4-diacetoxy-phenyl)-chromen-4-one

: 1394914-31-8
2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-((2-nitrobenzyl)oxy)-4H-chromen-4-one

Guidance literature:: Multi-step reaction with 3 steps

1: 1H-imidazole; thiophenol / 1-methyl-pyrrolidin-2-one / 0 - 20 °C

2: potassium carbonate / acetone / 20 °C

3: methanol; ammonia / 1 h / 0 °C

With 1H-imidazole; methanol; ammonia; potassium carbonate; thiophenol; In 1-methyl-pyrrolidin-2-one; acetone;
DOI:10.1007/s12272-012-0108-9