HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Butyryl-4-(2-methylphenylamino)8-hydroxyquinoline → 3-Butyryl-4-(2-methylphenylamino)-8-(2-methoxy-ethoxy)quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Butyryl-4-(2-methylphenylamino)8-hydroxyquinoline | HCID 10403732 | — |
| Reactant | 2-Methoxyethyl benzenesulfonate | HCID 11195284 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Butyryl-4-(2-methylphenylamino)-8-(2-methoxy-ethoxy)quinoline | HCID 11740395 | 38% |
Reaction Steps
A solution of 3-butyryl-4-(2-methylphenylamino)-8-hydroxyquinoline (3.20 g, 10 mmol) and potassium t-butoxide (1.47 g, 12 mmol) in dry tetrahydrofuran (100 ml) was heated at reflux for 5 minutes, then 2-methoxyethyl benzenesulphonate (4.33 g, 20 mmol) added and hearing continued for 18 hours. Evaporation of the solvent, chromatography (silica gel, 1-2% methanol in dichloromethane) and recrystallisation from ethyl acetate gave 3-butyryl-4-(2-methylphenylamino)-8-(2-methoxy-ethoxy)quinoline (1.42 g, 38%), m.p. 75°-77°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05432182 |
| Source dataset | uspto-grants-1995_07 |
| ORD ID | ord-03d2fb24306a4dd6b9c8534e684d301b |
| Source note | uspto-grants-1995_07 |