HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methoxyaniline → HCID 178450493, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methoxyaniline | HCID 7000 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | Ethyl 3-oxohexanoate | HCID 238498 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178450493 | HCID 178450493 | 27.2% |
Reaction Steps
A mixture of o-anisidine (22.6 ml, 0.2 mol), triethyl orthoformate (33.3 ml, 0.2 mol) and ethyl butyrylacetate (31.6 ml, 0.2 mol) was heated such that ethanol distilled over slowly. After 2.5 hours the mixture was allowed to cool, diluted with methanol (100 ml) and allowed to crystallise. The N-(2-methoxyphenyl)-2-butyryl-3-(2-methoxyphenylamino)acrylamide by-product was filtered off. Evaporation of the mother liquors and recrystallisation from petroleum ether (40-60) gave ethyl 2-butyryl-3-(2-methoxyphenylamino)acrylate (15.82 g, 27.2%), m.p. 74°-76°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04806550 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-dea392d7059746258a02ee999fe35fed |
| Source note | uspto-grants-1989_02 |