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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454136Generated: October 29, 2026

Methanol → 3-Fluoro-7-hydroxy-2-methylquinoline

https://huagongshe.com/reaction/454136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantBoron tribromideHCID 25134—
Reactant3-Fluoro-7-methoxy-2-methylquinolineHCID 22030792—
SolventDichloromethaneHCID 6344—
Product3-Fluoro-7-hydroxy-2-methylquinolineHCID 135763123—

Reaction Steps

3-Fluoro-7-methoxy-2-methylquinoline (0.16 g, 0.85 mmol) was taken up in dichloromethane (4 ml) under nitrogen and treated with boron tribromide solution (4 ml of a 1.0M solution in dichloromethane, 4.0 mmol). The reaction was stirred for 24 hours at ambient temperature followed by the slow addition of excess methanol. The solution was stirred for a further 2 hours and then evaporated to dryness to give 3-fluoro-7-hydroxy-2-methylquinoline which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492560B2
Source datasetuspto-grants-2013_07
ORD IDord-1671a113e0e84df59dd109665832c08a
Source noteuspto-grants-2013_07