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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051572Generated: October 26, 2026

Potassium Carbonate → 8-Fluoro-5-methoxy-2-methylquinoline

https://huagongshe.com/reaction/1051572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Fluoro-5-methoxyanilineHCID 13559075—
Reactant8-Chloro-5-methoxy-2-methylquinoline hydrochlorideHCID 75480717—
Reactant(S)-5-methoxy-2-methyl-1,2,3,4-tetrahydroquinolineHCID 118075405—
SolventDichloromethaneHCID 6344—
Product8-Fluoro-5-methoxy-2-methylquinolineHCID 11807582162%

Reaction Steps

8-Fluoro-5-methoxy-2-methylquinoline was synthesized from 2-fluoro-5-methoxyaniline (30.0 g, 213 mmol) according to the procedures described above for 8-chloro-5-methoxy-2-methylquinoline hydrochloride (Intermediate 1, Step 1) with the following change: The hydrochloride salt was dissolved in dichloromethane (400 mL) and the pH of the resulting solution was adjusted to 8-9 with saturated aqueous potassium carbonate solution. The resulting mixture was extracted with dichloromethane, and the combined organic layers were dried over anhydrous sodium sulfate, filtered, and concentrated under vacuum. The residue was purified via column chromatography on silica gel (eluting with 20% ethyl acetate-petroleum ether) to afford 8-fluoro-5-methoxy-2-methylquinoline (25.2 g, 62%) as a yellow solid. MS (ESI, pos. ion) m/z 192 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388161B2
Source datasetuspto-grants-2016_07
ORD IDord-56d47b0c1f1147ebb9c5b0a1c41bdf6a
Source noteuspto-grants-2016_07