HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → 8-Chloro-2-phenoxyquinoline-3-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,8-Dichloro-quinoline-3-carbaldehyde | HCID 14917125 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 8-Chloro-2-phenoxyquinoline-3-carbaldehyde | HCID 57707846 | — |
Reaction Steps
To a solution of 2,8-dichloroquinoline-3-carbaldehyde (1 eq) in DMF (0.25 M) was added phenol (1.5 eq) and K2CO3 (2.0 eq) at rt and the mixture was stirred for 3 h at rt. The mixture was diluted with water, extracted with EtOAc (2 times) and the combined organic layers were washed with water (2 times), dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude product was purified by column chromatography on a Redi-Sep™ column using 0 to 40% gradient of EtOAc in hexane to provide 8-chloro-2-phenoxyquinoline-3-carbaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08901135B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-523b3c304e9a43528f08e84cf82e7846 |
| Source note | uspto-grants-2014_12 |