HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N-Dimethylaniline → 4H-pyran-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | 2,2,6-Trimethyl-4H-1,3-dioxin-4-one | HCID 79368 | — |
| Reactant | HCID 365127 | HCID 365127 | — |
| Product | 4H-pyran-4-one | HCID 7968 | — |
| Product | 2-Pyridone | HCID 8871 | — |
Reaction Steps
In addition, the reaction for obtaining an 4-pyrone compound from 2,2,6-trimethyl-1,3-dioxin-4-one has been known. That is, T. Kato et al [Chem, Pharm. Bull., 30, 1315(1982)] studied on the reaction between amides or acetoacetyl derivatives thereof and 2,2,6-trimethyl-1,3-dioxin-4-one and reported that the reaction of N-formylacetoacetamide with 2,2,6-trimethyl-1,3-dioxin-4-one in the presence of N,N-dimethylaniline gave a pyridone compound as the main product and 4-pyrone compound as the by-product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04739083 |
| Source dataset | uspto-grants-1988_04 |
| ORD ID | ord-35d0be8732aa4ce7a354f5b9b963e699 |
| Source note | uspto-grants-1988_04 |