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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204206Generated: October 31, 2026

N-bromobutanimide → 8-Bromo-5-isopropoxy-quinoline

https://huagongshe.com/reaction/2204206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant5-IsopropoxyquinolineHCID 58550862—
SolventAcetonitrileHCID 6342—
Product8-Bromo-5-isopropoxy-quinolineHCID 5855097692%

Reaction Steps

To a solution of 5-isopropoxyquinoline (1.87 g, 10.0 mmol) in acetonitrile (100 mL) was added NBS (1.78 g, 10.0 mmol) at 0° C. The mixture was stirred at rt for 2 h before the solvent was removed. The residue was partitioned between EtOAc and H2O. The layers were separated and the organic layer was washed with brine, dried over MgSO4, and concentrated. The crude material was purified by column chromatography (0-10% EtOAc-Hex) to provide 8-bromo-5-isopropoxy-quinoline (92%) as a light brown solid. ESI-MS m/z calc 265.1, found 266.1 (M+1)+. Retention time: 1.44 minutes (3 min run).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365588B2
Source datasetuspto-grants-2016_06
ORD IDord-0102ff226cb343a095c3b66dbfb758ba
Source noteuspto-grants-2016_06