HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Dimethyl (4-methoxy-2-nitrophenyl)methylidenemalonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Dimethyl malonate | HCID 7943 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 4-Methoxy-2-nitrobenzaldehyde | HCID 357691 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Dimethyl (4-methoxy-2-nitrophenyl)methylidenemalonate | HCID 54325413 | 72% |
Reaction Steps
A mixture of 4-methoxy-2-nitrobenzaldehyde (21.3 g, Org. Synth., Vol. V, p-139, 1973), dimethyl malonate (16.5 g), piperidine (2.5 ml), and acetic acid (0.25 ml) in methanol (125 ml) was heated under reflux for 24 hr. The reaction mixture was concentrated, diluted with 1 N aqueous hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed with 10% aqueous potassium carbonate and saturated aqueous sodium chloride, dried, and concentrated. The residue was purified by silica gel column chromatography (eluent: ethyl acetate:hexane=1:2) to obtain the titled compound (25 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06310107B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-c39e045832394d2084be085ad4f9d311 |
| Source note | uspto-grants-2001_10 |