Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Quinoline | HCID 7047 | — |
| Reactant | HCID 21419824 | HCID 21419824 | — |
| Reactant | Methylorthoformate | HCID 53629101 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 68125247 | HCID 68125247 | 58.5% |
Reaction Steps
11.7 g of methyl orthoformate were added to a solution of 23.4 g of m-acetamido-acetylacetanilide in 250 ml of anhydrous methanol and the mixture was refluxed for 3 hours and cooled. 0.6 ml of quinoline were added thereto and the methanol was distilled off under reduced pressure. Toluene was added to the residue and the mixture was heated at 140° C. for one hour while distilling a methanol-toluene azeotrope. The mixture was then concentrated to dryness under reduced pressure and the residue was chromatographed over silica gel. Elution with ethyl acetate yielded 14.5 g of m-acetamido-3-methoxy-crotonanilide melting at 167° C. Crystallization from acetone did not change the melting point.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04039316 |
|---|
| Source dataset | uspto-grants-1977_08 |
|---|
| ORD ID | ord-2c46b7b8524d41cb8729585649132d93 |
|---|
| Source note | uspto-grants-1977_08 |
|---|