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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384436Generated: October 31, 2026

Thionyl Chloride → HCID 59527509, compound

https://huagongshe.com/reaction/384436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 59527017HCID 59527017—
CatalystPyridineHCID 1049—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59527509HCID 59527509—

Reaction Steps

[4-(Benzyloxy)-6-fluoro-3-methylquinolin-2-yl]methanol (4.02 g) was dissolved in THF (50 mL) and toluene (50 mL), and 10 drops of pyridine were added thereto. Thionyl chloride (1.50 mL) was gradually added dropwise thereto under ice-cooling, and the reaction mixture was stirred at the same temperature for 1 hour, and further stirred at room temperature for 1 hour. After the precipitated solid was collected by filtration, ethyl acetate and a saturated aqueous sodium hydrogen carbonate solution were gradually added with stirring to the filtrate under ice-cooling. After the foaming became stable, the organic layer was separated, washed sequentially with water and saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated. The residue was purified by silica gel column chromatography (eluent: chloroform) to obtain 4-(benzyloxy)-2-(chloromethyl)-6-fluoro-3-methylquinoline (3.85 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367702B2
Source datasetuspto-grants-2013_02
ORD IDord-9bbb5d6b2e47442b869dab4c62579224
Source noteuspto-grants-2013_02