HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 178418479, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Oxo-1lambda~5~-pyridine-2,5-dicarboxylic acid | HCID 13643503 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 178418479 | HCID 178418479 | 79.1% |
Reaction Steps
20.4 g of acetic acid anhydride (0.2 mole), 20.2 g of Et3N (0.2 mole) and 50 ml of CCl4 were put up in a flask. 18.3 g of isocinchomeronic acid-N-oxide (0.1 mole) was added by portions to this solution. The temperature rose to 50° C. After completion of the reaction the solvents were distilled off. About 100 ml of 20 percent KOH was added drop by drop to the viscous residue and the acetate was saponified over a 15 minute period at 80° C. After removal of the Et3N by extraction, the aqueous solution was acidified with concentrated HCl. The precipitate was sucked off, washed with water and dried under a vacuum. 11.0 g of 6-hydroxy nicotinic acid was obtained, which was pure according to NMR. The crude yield was about 79 percent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04609734 |
| Source dataset | uspto-grants-1986_09 |
| ORD ID | ord-52e57b3012044058a486db30d64d6456 |
| Source note | uspto-grants-1986_09 |