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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430090Generated: October 31, 2026

Ethyl Acetate → 2,5-Dichloro-4-methoxyquinoline

https://huagongshe.com/reaction/430090

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant2,4,5-TrichloroquinolineHCID 18353668—
ReactantHCID 178502595HCID 178502595—
SolventMethanolHCID 887—
Product2,5-Dichloro-4-methoxyquinolineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06320051B1
Source datasetuspto-grants-2001_11
ORD IDord-92851fa35ffa4a28b7a52e576c33192d
Source noteuspto-grants-2001_11