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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338945Generated: October 29, 2026

Ethyl Bromide → 7-Ethoxy-6-fluoro-2-methylquinoline

https://huagongshe.com/reaction/338945

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
ReactantPotassium CarbonateHCID 11430—
Reactant6-Fluoro-2-methylquinolin-7-olHCID 136338075—
SolventAcetoneHCID 180—
Product7-Ethoxy-6-fluoro-2-methylquinolineHCID 7098321865.7%

Reaction Steps

6-fluoro-2-methylquinolin-7-ol (500 mg, 1.41 mmol) (Example 119, Step B), potassium carbonate (585 mg, 4.23 mmol) and bromoethane (308 mg, 2.82 mmol) in acetone (10 mL) were stirred at 70° C. in a sealed tube for 20 hours. After dilution with water (50 mL) the reaction was extracted with DCM. The organic phases were concentrated and the residue purified by reverse phase chromatography (SP4, 25M, eluting with a gradient of water/ACN 100:0 to 0:100, 20 column volumes) to yield 7-ethoxy-6-fluoro-2-methylquinoline (190 mg, 65.6% yield) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889704B2
Source datasetuspto-grants-2014_11
ORD IDord-8bed541d5c104de78e648d9f01b8f606
Source noteuspto-grants-2014_11