HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 2,5-Dichloro-4-methoxyquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2,4,5-Trichloroquinoline | HCID 18353668 | — |
| Reactant | HCID 178502595 | HCID 178502595 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2,5-Dichloro-4-methoxyquinoline | HCID 18353703 | — |
Reaction Steps
To 2.4,5-trichloroquinoline (0.79 g, 3.4 mmol) was added KOMe (20.4 ml of a 0.5 M suspension in MeOH). The mixture was heated under reflux for 2.5 h. EtOAc was added and the solution was allowed to cool to room temperature. The solvent was evaporated in vacuo and the residue submitted to column chromatography (silica gel, EtOAc:hexanes 1:6→1:3). 4,5-Dichloro-2-methoxyquinoline eluted first, then 2,4,5-trichloroquinoline. followed by the title compound, a colourless solid, (0.43 g, 44%). δH (CDCl3) 4.04 (s, 3H), 6.77 (s, 1H), 7.50-7.60 (m, 2H), 7.85 (dd, J=6.7, 3.0, 1H); MS (AP+) 228 (MH+, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06320051B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-92851fa35ffa4a28b7a52e576c33192d |
| Source note | uspto-grants-2001_11 |