5-(benzyloxy)-2-(3,4-bis(benzyloxy)phenyl)-4-oxo-4H-chromen-7-yl-4-methylbenzenesulfonate

Base Information

• Chemical Name: 5-(benzyloxy)-2-(3,4-bis(benzyloxy)phenyl)-4-oxo-4H-chromen-7-yl-4-methylbenzenesulfonate
• CAS No.: 1610737-90-0
• Molecular Formula: C₄₃H₃₄O₈S
• Molecular Weight: 710.804
• Mol file: 1610737-90-0.mol

Synonyms:5-(benzyloxy)-2-(3,4-bis(benzyloxy)phenyl)-4-oxo-4H-chromen-7-yl-4-methylbenzenesulfonate

Chemical Property of 5-(benzyloxy)-2-(3,4-bis(benzyloxy)phenyl)-4-oxo-4H-chromen-7-yl-4-methylbenzenesulfonate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 5-(benzyloxy)-2-(3,4-bis(benzyloxy)phenyl)-4-oxo-4H-chromen-7-yl-4-methylbenzenesulfonate

There total 5 articles about 5-(benzyloxy)-2-(3,4-bis(benzyloxy)phenyl)-4-oxo-4H-chromen-7-yl-4-methylbenzenesulfonate 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: 80.0%

2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-yl-4-methylbenzenesulfonate (1610737-88-6) + benzyl bromide (100-39-0) → 5-(benzyloxy)-2-(3,4-bis(benzyloxy)phenyl)-4-oxo-4H-chromen-7-yl-4-methylbenzenesulfonate (1610737-90-0)

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 12h; Inert atmosphere;

DOI:10.1016/j.bmc.2014.04.016

Reference yield:

4-(5-acetoxy-4-oxo-7-(tosyloxy)-4H-chromen-2-yl)-1,2-phenylene diacetate (1610737-84-2) → 5-(benzyloxy)-2-(3,4-bis(benzyloxy)phenyl)-4-oxo-4H-chromen-7-yl-4-methylbenzenesulfonate (1610737-90-0)

Guidance literature:

Multi-step reaction with 2 steps

1: ammonia / methanol / 2 h / 20 °C

2: potassium carbonate / N,N-dimethyl-formamide / 12 h / 20 °C / Inert atmosphere

With ammonia; potassium carbonate; In methanol; N,N-dimethyl-formamide;

DOI:10.1016/j.bmc.2014.04.016

Reference yield:

luteolin tetraacetate (1061-93-4) → 5-(benzyloxy)-2-(3,4-bis(benzyloxy)phenyl)-4-oxo-4H-chromen-7-yl-4-methylbenzenesulfonate (1610737-90-0)

Guidance literature:

Multi-step reaction with 4 steps

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

2: triethylamine / tetrahydrofuran / 8 h / 20 °C

3: ammonia / methanol / 2 h / 20 °C

4: potassium carbonate / N,N-dimethyl-formamide / 12 h / 20 °C / Inert atmosphere

With 1H-imidazole; ammonia; potassium carbonate; thiophenol; triethylamine; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; methanol; N,N-dimethyl-formamide;

DOI:10.1016/j.bmc.2014.04.016

upstream raw materials:

luteolin tetraacetate

4-(5-acetoxy-4-oxo-7-(tosyloxy)-4H-chromen-2-yl)-1,2-phenylene diacetate

2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-yl-4-methylbenzenesulfonate

benzyl bromide

Downstream raw materials:

2-(3,4-dihydroxyphenyl)-5-hydroxy-7-morpholino-4H-chromen-4-one

5-(benzyloxy)-2-(3,4-bis(benzyloxy)phenyl)-7-morpholino-4H-chromen-4-one