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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2280999Generated: October 25, 2026

8-Methylquinoline → 5-Bromo-8-methylquinoline

https://huagongshe.com/reaction/2280999

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-MethylquinolineHCID 11910—
ReactantBromineHCID 24408—
CatalystHCID 178418844HCID 178418844—
SolventSulfuric AcidHCID 1118—
Product5-Bromo-8-methylquinolineHCID 471502292.4%

Reaction Steps

To a solution of 8-Metyl quinoline (30 g, 0.209 mol) in Conc.H2SO4 (300 ml) was added Silver sulphate (97.98 g, 0.314 mol) in lots at 0° C. and followed by Bromine (10.74 ml, 0.209 mol) drop wise for 10 min. After addition of Bromine, the reaction mixture was stirred at RT for 4 h and the reaction completion was confirmed by TLC. After completion of reaction the reaction mixture was quenched with ice and basified with NH4OH solution and extracted with ethyl acetate. The organic layer was washed with water, brine solution and dried over anhydrous sodium sulphate and concentrated to afford (43 g, 92.4% yield) as dark brown liquid. The crude product was as such taken for next step without further purification. 1H NMR (DMSO-d6 400 MHz): δ 8.97-8.96 (dd, J=4.16, 5.8 Hz, 1H), 8.45-8.42 (dd, J=8.56, 10.2 Hz, 1H), 7.81-7.79 (d, J=7.68 Hz, 1H), 7.67-7.64 (dd, J˜8.52, 12.64 Hz, 1H), 7.53-7.51 (dd, J=7.64, 8.52 Hz, 1H), 2.66 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139568B2
Source datasetuspto-grants-2015_09
ORD IDord-66a43ba4336e4b5e942e34be8bdf21bf
Source noteuspto-grants-2015_09