HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → HCID 178469510, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Diethyl (ethoxymethylene)malonate | HCID 6871 | — |
| Reactant | Biphenyl | HCID 7095 | — |
| Reactant | Diphenyl Ether | HCID 7583 | — |
| Product | HCID 178469510 | HCID 178469510 | — |
Reaction Steps
In step 1 of sequence A, an aniline, substituted by the appropriate R2 group or groups, is condensed with a dialkyl alkoxymethylenemalonate such as diethyl ethoxymethylenemalonate by heating at 120° to 150°C. The intermediate formed is condensed by heating at a temperature of 150° to 300°C. in a high boiling inert solvent such as diphenyl ether or mixtures of diphenyl ether and biphenyl (e.g. Dowtherm A) to give the ethyl 4-hydroxyquinoline-3-carboxylate product of step 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03976651 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-e782a77e399d468e8f9d99ca978ecee5 |
| Source note | uspto-grants-1976_08 |