HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 70432961, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Methyl 4-aminobenzoate | HCID 12082 | — |
| Reactant | Propionic acid, 2-benzoyl-, ethyl ester | HCID 139166 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Diphenyl Ether | HCID 7583 | — |
| Product | HCID 70432961 | HCID 70432961 | 28.1% |
Reaction Steps
Ethyl alpha-methylbenzoylacetate (5 grams) and 3.67 grams of methyl p-aminobenzoate are dehydrated (by heating) for three days in 100 ml of chloroform in the presence of 0.7 gram of p-toluenesulfonic acid. p-Toluenesulfonic acid is removed therefrom, the filtrate is concentrated, and purified by silica gel column chromatography to give an oil. The resulting oily product is heated to reflux in 70 ml of diphenyl ether, cooled, and crystals which separate therefrom are collected by filtration and recrystallized from a mixture of dimethyl formamide and water to give 2 grams of methyl 3-methyl-2-phenyl-4-quinolone-6-carboxylate, colorless crystals, melting point above 300° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04711898 |
| Source dataset | uspto-grants-1987_12 |
| ORD ID | ord-1f427f43fd904877a26da0de847b3ab7 |
| Source note | uspto-grants-1987_12 |