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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666664Generated: October 31, 2026

Boron tribromide → 2-Chloro-4-methyl-quinolin-6-ol

https://huagongshe.com/reaction/1666664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
Reactant2-Chloro-6-methoxy-4-methylquinolineHCID 224788—
ReactantSodium BicarbonateHCID 516892—
SolventDichloromethaneHCID 6344—
Product2-Chloro-4-methyl-quinolin-6-olHCID 76638280.4%

Reaction Steps

A solution of 2-chloro-6-methoxy-4-methylquinoline (0.20 g) in dichloromethane (15 mL) was cooled to −78° C., followed by addition of a solution (5.3 mL) of 1 M boron tribromide in dichloromethane, and the mixture was stirred for 12 h while slowly heating to room temperature. To the reaction mixture was added a saturated sodium hydrogencarbonate solution to make it basic, and the mixture was extracted with chloroform. The aqueous layer was reextracted with a mixture solution of ethyl acetate and n-butanol, then the organic layer was combined and concentrated under reduced pressure, and the resulting solids were washed with diethyl ether to obtain 2-chloro-6-hydroxy-4-methylquinoline (0.15 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044068B2
Source datasetuspto-grants-2011_10
ORD IDord-a3f835033b6041bb9711c03341fcb6e9
Source noteuspto-grants-2011_10