HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207016Generated: October 25, 2026
Potassium Hydroxide → 5-Bromo-6-methoxy-7-methylquinoline
https://huagongshe.com/reaction/2207016
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 6-Methoxy-7-methylquinoline | HCID 15534898 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 5-Bromo-6-methoxy-7-methylquinoline | HCID 66630714 | — |
Reaction Steps
To the solution of 6-methoxy-7-methylquinoline (4.28 g, 24.6 mmol) in 50 mL of concentrated H2SO4 was added N-bromosuccinimide (4.41 g, 14.6 mmol) at 15° C., and the reaction was stirred at 15° C. for 3.5 hours. The reaction mixture was poured into ice-water (600 mL). The aqueous mixture was adjusted with a 50% KOH solution to pH ˜10, and then extracted with DCM (3×). The combined extract was dried with sodium sulfate. Concentration under reduced pressure gave 5-bromo-6-methoxy-7-methylquinoline. LCMS-ESI+ (m/z): 252.1, 254.1 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09376392B2 |
|---|
| Source dataset | uspto-grants-2016_06 |
|---|
| ORD ID | ord-5ec83fbf657d4377aa8c656de182dfa7 |
|---|
| Source note | uspto-grants-2016_06 |
|---|