HuagongsheHuagongshe Chemistry Print Report · For research reference only
4,7-Dichloroquinoline → 7-Chloro-4-(4-fluorophenoxy)quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4,7-Dichloroquinoline | HCID 6866 | — |
| Reactant | 4-Fluorophenol | HCID 9732 | — |
| Reactant | 4-Pyrrolidinopyridine | HCID 75567 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 7-Chloro-4-(4-fluorophenoxy)quinoline | HCID 164171 | 649.9% |
Reaction Steps
To a 50 mL flask equipped with a condenser, drying tube and thermometer, was added 1.98 g (0.01 moles) of 4,7-dichloroquinoline, 1.57 g (0.0014 moles) of 4-fluorophenol, 0.22 g (0.0015 moles) of 4-pyrrolidinopyridine and 20 mL of xylene. The reaction mixture was heated to reflux and reaction progress was monitored by TLC. After 18 hr, the mixture was cooled and washed with 50 mL of 5 N NaOH. The caustic layer was extracted with 3×20 mL of diethyl ether. The xylene and the ether layers were combined and dried over Na2SO4. Removal of the solvent provided 2.49 g (91 percent yield) of product, mp=88°-91° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05245036 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-083e912021ea4636b30489d9253b9684 |
| Source note | uspto-grants-1993_09 |