HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methane → 5-acetyl-6-methyl-2(1H)-pyridinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | 5-Acetyl-6-methyl-2-oxo-1,2-dihydropyridine-3-carboxylic acid | HCID 13232040 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 5-acetyl-6-methyl-2(1H)-pyridinone | HCID 4421736 | — |
Reaction Steps
C-1. 5-Acetyl-6-methyl-2(1H)-pyridinone--A 10 g portion of 5-acetyl-1,2-dihydro-6-methyl-2-oxonicotinic acid was heated neat in a bath of a boiling mixture of diphenyl and diphenyl ether for 40 minutes and the mixture allowed to cool to room temperature. The reaction mixture was dissolved in hot isopropyl alcohol, treated with decolorizing charcoal and filtered, and the filtrate allowed to stand at room temperature for several hours. The separated product was collected and dried at 90°-95° C. to yield 4.3 g of 5-acetyl-6-methyl-2-(1H)-pyridinone, m.p. 193°-195° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04517190 |
| Source dataset | uspto-grants-1985_05 |
| ORD ID | ord-2ebe0c1659494fc595566aa11daa9fee |
| Source note | uspto-grants-1985_05 |