HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(2-Cyanoethyl)benzaldehyde → 4-hydroxy-3-[3-[3-(2-cyanoethyl)phenyl]-1-oxo-2-propenyl]-1,6-dimethyl-2(1H)-pyridinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(2-Cyanoethyl)benzaldehyde | HCID 11499259 | — |
| Reactant | 2(1H)-Pyridone, 3-acetyl-4-hydroxy-1,6-dimethyl- | HCID 54691703 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-hydroxy-3-[3-[3-(2-cyanoethyl)phenyl]-1-oxo-2-propenyl]-1,6-dimethyl-2(1H)-pyridinone | HCID 136344263 | 46.7% |
Reaction Steps
According to the same manner as that of Example a-1 except that 0.74 g of 3-(2-cyanoethyl)benzaldehyde was used in place of 3-[(methoxycarbonyl)methoxy]benzaldehyde, 0.93 g of 3-acetyl-4-hydroxy-1,6-dimethyl-2(1H)-pyridinone was used in place of 3-acetyl-4-hydroxy-6-methyl-2(1H)-pyridinone, and 8 ml of ethanol was used in place of pyridine, 0.70 g of 4-hydroxy-3-[3-[3-(2-cyanoethyl)phenyl]-1-oxo-2-propenyl]-1,6-dimethyl-2(1H)-pyridinone [Compound No. (106a)] was obtained as a yellow crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07989478B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-867e9bd47b7d401abb580c5eb84465e6 |
| Source note | uspto-grants-2011_08 |