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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791657Generated: November 4, 2026

Thionyl Chloride → 2-Chloro-3-fluoro-7-methoxyquinoline

https://huagongshe.com/reaction/1791657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant3-fluoro-7-methoxyquinolin-2(1H)-oneHCID 15260580—
CatalystDimethylformamideHCID 6228—
Product2-Chloro-3-fluoro-7-methoxyquinolineHCID 2203059197%

Reaction Steps

3-Fluoro-7-methoxyquinol-2(1H)-one (300 mg, 1.55 mmol), (prepared as in Tetrahedron, Vol. 52, No. 9, pp. 3223–3228, 1996), was dissolved in thionyl chloride (3 ml), treated with DMF (1 drop) and heated at reflux for 1 hour. The excess thionyl chloride was removed by evaporation and the residue azeotroped with toluene (3×). The residue was basified to pH8 with saturated aqueous sodium hydrogen carbonate solution and extracted with ethyl acetate (3×20 ml). The organic solution was washed with water and brine then dried (MgSO4) and evaporated to dryness to give 2-chloro-3-fluoro-7-methoxyquinoline (320 mg, 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074800B1
Source datasetuspto-grants-2006_07
ORD IDord-e66ac03e03f84c75ad3ea3256f26e11f
Source noteuspto-grants-2006_07