HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → 6-Hydroxyquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Aniline | HCID 6115 | — |
| Reactant | 1,2-Dihydroquinazolin-2-one | HCID 344381 | — |
| Reactant | 6-(Benzyloxy)-4-chloroquinoline | HCID 23078431 | — |
| Solvent | 1,2-Dichlorobenzene | HCID 7239 | — |
| Product | 6-Hydroxyquinoline | HCID 11374 | — |
Reaction Steps
A 6-benzyloxy-4-chloroquinoline derivative or a corresponding quinazolone derivative is reacted with a phenol derivative or a corresponding aniline derivative in a suitable solvent, for example, o-dichlorobenzene, or in the absence of a solvent, for example, at 120 to 180° C. (step (i) above). Next, a 6-hydroxyquinoline derivative may be produced by reacting the resultant compound with a suitable acid, for example, methanesulfonic acid/trifluoroacetic acid (step (ii) above). The contemplated compound may be produced by reacting the 6-hydroxyquinoline derivative with an alkylating agent, for example, 1-bromo-2-chloroethane (step (iii) above).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07560558B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-3615413c83c24974ad40d55b6c6e41b8 |
| Source note | uspto-grants-2009_07 |