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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720320Generated: October 28, 2026

Thionyl Chloride → HCID 21891598, compound

https://huagongshe.com/reaction/720320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 21891575HCID 21891575—
SolventDichloromethaneHCID 6344—
ProductHCID 21891598HCID 21891598—

Reaction Steps

Thionyl chloride (1.7 mL) was added to a solution of 2-hydroxymethyl-5,6,7-trimethoxyquinoline (1.45 g) in dichloromethane (15 mL) under ice cooling, and the mixture was stirred at room temperature for 30 minutes. After concentrating the reaction mixture under reduced pressure, an aqueous solution of potassium carbonate was added to the residue to alkalify it. The thus-treated residue was extracted with diethyl ether. The resultant organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure, and the residue was purified by column chromatography on silica gel (ethyl acetate:hexane=1:2) to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135473B2
Source datasetuspto-grants-2006_11
ORD IDord-e4368a7d227345d9afc744270f4b5076
Source noteuspto-grants-2006_11