3-(6-methoxy-2-methyl-4-oxo-4H-chromen-3-yl methyl)benzoic acid methyl ester

Base Information

Chemical Name:3-(6-methoxy-2-methyl-4-oxo-4H-chromen-3-yl methyl)benzoic acid methyl ester
CAS No.:160891-98-5
Molecular Formula:C₂₀H₁₈O₅
Molecular Weight:338.36
Hs Code.:

Synonyms:3-(6-methoxy-2-methyl-4-oxo-4H-chromen-3-yl methyl)benzoic acid methyl ester

Suppliers and Price of 3-(6-methoxy-2-methyl-4-oxo-4H-chromen-3-yl methyl)benzoic acid methyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 3-(6-methoxy-2-methyl-4-oxo-4H-chromen-3-yl methyl)benzoic acid methyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 3-(6-methoxy-2-methyl-4-oxo-4H-chromen-3-yl methyl)benzoic acid methyl ester

There total 5 articles about 3-(6-methoxy-2-methyl-4-oxo-4H-chromen-3-yl methyl)benzoic acid methyl ester 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:

: 65547-82-2
2'-benzyloxy-5'-methoxyacetophenone

: 160891-98-5
3-(6-methoxy-2-methyl-4-oxo-4H-chromen-3-yl methyl)benzoic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) sodium methoxide / 1.) methanol, RT, 20 min, 2.) methanol, RT, 18 h

2: 80 percent / H₂ / 5percent Pd/C / tetrahydrofuran / 3 h / 1034.3 Torr / Ambient temperature

3: 97 percent / triethylamine, dimethylaminopyridine / CH₂Cl₂ / 1 h / Ambient temperature

4: 1.) sodium hydride, 2.) glacial acetic acid, hydrochloric acid / 1.) DMSO, 20 deg C, 1 h, 2.) reflux, 30 min

With hydrogenchloride; dmap; hydrogen; sodium methylate; sodium hydride; acetic acid; triethylamine; palladium on activated charcoal; In tetrahydrofuran; dichloromethane;
DOI:10.1002/jhet.5570310617

Reference yield:

: 52178-50-4
Methyl 3-formylbenzoate

: 160891-98-5
3-(6-methoxy-2-methyl-4-oxo-4H-chromen-3-yl methyl)benzoic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) sodium methoxide / 1.) methanol, RT, 20 min, 2.) methanol, RT, 18 h

2: 80 percent / H₂ / 5percent Pd/C / tetrahydrofuran / 3 h / 1034.3 Torr / Ambient temperature

3: 97 percent / triethylamine, dimethylaminopyridine / CH₂Cl₂ / 1 h / Ambient temperature

4: 1.) sodium hydride, 2.) glacial acetic acid, hydrochloric acid / 1.) DMSO, 20 deg C, 1 h, 2.) reflux, 30 min

With hydrogenchloride; dmap; hydrogen; sodium methylate; sodium hydride; acetic acid; triethylamine; palladium on activated charcoal; In tetrahydrofuran; dichloromethane;
DOI:10.1002/jhet.5570310617

Reference yield:

: 3-<3-(2-benzyloxy-5-methoxyphenyl)-3-oxopropenyl>benzoic acid methyl ester

: 160891-98-5
3-(6-methoxy-2-methyl-4-oxo-4H-chromen-3-yl methyl)benzoic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 80 percent / H₂ / 5percent Pd/C / tetrahydrofuran / 3 h / 1034.3 Torr / Ambient temperature

2: 97 percent / triethylamine, dimethylaminopyridine / CH₂Cl₂ / 1 h / Ambient temperature

3: 1.) sodium hydride, 2.) glacial acetic acid, hydrochloric acid / 1.) DMSO, 20 deg C, 1 h, 2.) reflux, 30 min

With hydrogenchloride; dmap; hydrogen; sodium hydride; acetic acid; triethylamine; palladium on activated charcoal; In tetrahydrofuran; dichloromethane;
DOI:10.1002/jhet.5570310617