HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 54547794, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 4-Pyridinecarboxaldehyde | HCID 13389 | — |
| Reactant | HCID 14027755 | HCID 14027755 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 54547794 | HCID 54547794 | 44.1% |
Reaction Steps
To 0.7 g of 1-(4-fluorophenyl)-6-methyl-4-oxo-1,4-dihydronicotinic acid was added 0.33 g of isonicotinaldehyde and 0.61 g of acetic anhydride, and they were refluxed for 5 hours. After completion of the reaction, 30 ml of water was added to the reaction mixture, and the mixture was successively extracted with three 30-ml portions of chloroform. The chloroform layer was separated, washed with 20 ml of a saturated aqueous solution of sodium chloride, and then dried with anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure to obtain 0.42 g of 1-(4-fluorophenyl)-6-[2-(pyridin-4-yl)ethenyl]-4-oxo-1,4-dihydronicotinic acid having a melting point of 205°-215° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04698352 |
| Source dataset | uspto-grants-1987_10 |
| ORD ID | ord-91e4ca6d55aa415fa706c6b223c9cbf9 |
| Source note | uspto-grants-1987_10 |