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
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 7-Methoxy-6-methylquinoline | HCID 59366165 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 8-Bromo-7-methoxy-6-methylquinoline | HCID 59366188 | 67% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853202B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-1293a097435f4c13a444c7ad2bc925e1 |
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| Source note | uspto-grants-2014_10 |
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