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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 931744Generated: October 25, 2026

Methanol → 5-Bromo-6-hydroxy-7-methyl-quinoline

https://huagongshe.com/reaction/931744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantBoron tribromideHCID 25134—
Reactant5-Bromo-6-methoxy-7-methylquinolineHCID 66630714—
SolventDichloromethaneHCID 6344—
Product5-Bromo-6-hydroxy-7-methyl-quinolineHCID 2307830981.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To the solution of 5-bromo-6-methoxy-7-methylquinoline (6.5 g, 25.8 mmol) in DCM (150 mL) was added BBr3 slowly (77.3 mL, 1.0 M in DCM, 77.3 mmol). The mixture was stirred for 3 hours and cooled to 0° C. Methanol (40 mL) was added slowly and the mixture was stirred for 20 minutes. The solvents were removed under reduced pressure. The solid was dissolved in methanol (100 mL) and was treated with 1.0 N sodium hydroxide solution (50 mL) (pH ˜12). The mixture was stirred for 12 hours and acetic acid was added to adjust pH to between 4-5. The mixture was filtered and washed with water. The gray solid was dried under reduced pressure to give 5-bromo-7-methylquinolin-6-ol (5.0 g). LCMS-ESI+ (m/z): 238.2, 240.1 (M+H)+, 236.1, 238.0 (M−H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296758B2
Source datasetuspto-grants-2016_03
ORD IDord-7bac8e3398b043f1b0b7d5374a40c5b2
Source noteuspto-grants-2016_03