methyl 6,7-dimethyl-2-(4-methyl-3-nitrophenyl)-4-oxo-4H-chromene-8-carboxylate

Base Information

Chemical Name:methyl 6,7-dimethyl-2-(4-methyl-3-nitrophenyl)-4-oxo-4H-chromene-8-carboxylate
CAS No.:1400816-00-3
Molecular Formula:C₂₀H₁₇NO₆
Molecular Weight:367.358
Hs Code.:

Synonyms:methyl 6,7-dimethyl-2-(4-methyl-3-nitrophenyl)-4-oxo-4H-chromene-8-carboxylate

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Chemical Property of methyl 6,7-dimethyl-2-(4-methyl-3-nitrophenyl)-4-oxo-4H-chromene-8-carboxylate

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Technology Process of methyl 6,7-dimethyl-2-(4-methyl-3-nitrophenyl)-4-oxo-4H-chromene-8-carboxylate

There total 4 articles about methyl 6,7-dimethyl-2-(4-methyl-3-nitrophenyl)-4-oxo-4H-chromene-8-carboxylate 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: 73.0%

: 6,7-dimethyl-2-(4'-methyl-3'-nitrophenyl)-4-oxo-4H-1-benzopyran-8-carboxylic acid

: 18107-18-1
diazomethyl-trimethyl-silane

: 1400816-00-3
methyl 6,7-dimethyl-2-(4-methyl-3-nitrophenyl)-4-oxo-4H-chromene-8-carboxylate

Guidance literature:: In methanol; diethyl ether; at 20 ℃; for 24h;
DOI:10.1016/j.ejmech.2012.07.028

Reference yield:

: 1400815-83-9
C₁₉H₁₆N₂O₅

: 1400816-00-3
methyl 6,7-dimethyl-2-(4-methyl-3-nitrophenyl)-4-oxo-4H-chromene-8-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: pyridine; potassium hydroxide / Heating

1.2: Reflux

2.1: Acidic conditions

3.1: methanol; diethyl ether / 24 h / 20 °C

With pyridine; potassium hydroxide; In methanol; diethyl ether;
DOI:10.1016/j.ejmech.2012.07.028

Reference yield:

: 89638-56-2
3-cyano-4,5-dimethyl-2-hydroxyacetophenone

: 1400816-00-3
methyl 6,7-dimethyl-2-(4-methyl-3-nitrophenyl)-4-oxo-4H-chromene-8-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: triethylamine / 1,4-dioxane

2.1: pyridine; potassium hydroxide / Heating

2.2: Reflux

3.1: Acidic conditions

4.1: methanol; diethyl ether / 24 h / 20 °C

With pyridine; triethylamine; potassium hydroxide; In 1,4-dioxane; methanol; diethyl ether;
DOI:10.1016/j.ejmech.2012.07.028