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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853441Generated: October 25, 2026

Thionyl Chloride → Methyl 7-(benzyloxy)-4-chloro-6-quinolinecarboxylate

https://huagongshe.com/reaction/853441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantMethyl 7-(benzyloxy)-4-oxo-1,4-dihydro-6-quinolinecarboxylateHCID 22936245—
SolventDimethylformamideHCID 6228—
ProductMethyl 7-(benzyloxy)-4-chloro-6-quinolinecarboxylateHCID 22936661—

Reaction Steps

After adding thionyl chloride (70 ml) and a catalytic amount of dimethylformamide to methyl 7-(benzyloxy)-4-oxo-1,4-dihydro-6-quinolinecarboxylate (7.19 g, 23.2 mmol), the mixture was heated to reflux for 3 hours while stirring. The reaction solution was concentrated under reduced pressure, a 2N sodium hydroxide solution was gradually added for neutralization, extraction was performed with ethyl acetate, and the organic layer was washed with water and saturated brine and dried over anhydrous sodium sulfate. The solvent was distilled off, diethyl ether was added for crystallization, and the crystals were filtered out and blow-dried to obtain the title compound (4.067 g, 12.4 mmol) as light brown crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253286B2
Source datasetuspto-grants-2007_08
ORD IDord-9c0f573d170143539cb201886186ceb3
Source noteuspto-grants-2007_08