Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Pyridine | HCID 1049 | — |
| Edukt | 4-Nitrophenyl trifluoroacetate | HCID 69569 | — |
| Edukt | HCID 178422970 | HCID 178422970 | — |
| Produkt | HCID 178432383 | HCID 178432383 | — |
Reaktionsschritte
A mixture of 1 g of 4-hydroxy-7-methyl-1,8-naphthyridine-3-carboxylic acid and 25 ml of anhydrous pyridine was heated on an oil bath at 50 to 60°C while stirring. Then, 1.38 g of p-nitrophenyl trifluoroacetate were added thereto and, after the heating was interrupted, stirring was carried out for 2 hours. The precipitated crystals were collected by filtration and washed with ethanol to give 4-hydroxy--methyl--methyl-1,8-naphthyridine-3-carboxylic acid p-nitrophenyl ester as pale yellow crystalline powder melting at 311 to 313°C (decomp.). Yield, 1.2 g. IR νC=0 1700 cm-1 ; νNO2 1520 cm-1, 1345 cm-1.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US03954733 |
|---|
| Quelldatensatz | uspto-grants-1976_05 |
|---|
| ORD ID | ord-d026d38346d84915ae3f8aafb3a3a39f |
|---|
| Quellennotiz | uspto-grants-1976_05 |
|---|