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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 532842Generated: October 30, 2026

N-bromobutanimide → 8-Bromo-7-methoxy-6-methylquinoline

https://huagongshe.com/reaction/532842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant7-Methoxy-6-methylquinolineHCID 59366165—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product8-Bromo-7-methoxy-6-methylquinolineHCID 5936618867%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirred solution of 6-methyl-7-methoxy-quinoline (3.0 g, 17.3 mmol) in DMF (20 ml) was added NBS (3.4 g, 19 mmol). The resulting suspension was stirred for 3 h at 60° C. and monitored by LCMS. The reaction mixture was diluted with EtOAc (100 ml) and filtered. The organic layer was washed with saturated aqueous NaHCO3 and brine, dried over Na2SO4 and then purified by flash column chromatography on silica gel to give the desired product (2.9 g, 67%). MS (ES) m/z 251.6 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853202B2
Source datasetuspto-grants-2014_10
ORD IDord-1293a097435f4c13a444c7ad2bc925e1
Source noteuspto-grants-2014_10