HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 1-phenyl-8-fluoro-3-bromomethyl-2(1H)-quinolone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Benzyl Peroxide | HCID 11229634 | — |
| Reactant | 1-phenyl-8-fluoro-3-methyl-2(1H)-quinolone | HCID 19021639 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 1-phenyl-8-fluoro-3-bromomethyl-2(1H)-quinolone | HCID 19021638 | — |
Reaction Steps
Reflux a solution of 1-phenyl-8-fluoro-3-methyl-2(1H)-quinolone (0.54 g), N-bromosuccinimide (0.38 g) and benzyl peroxide (0.04 g) in dry benzene (11 mL) for 6 hours. Evaporate, partition between dichloromethane and water, dry and evaporate the organic phase, and dry the residue at room temperature and high vacuum to obtain 1-phenyl-8-fluoro-3-bromomethyl-2(1H)-quinolone, suitable for further reactions (see example 32).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05064837 |
| Source dataset | uspto-grants-1991_11 |
| ORD ID | ord-ee17bcea0df042cf9a84a2834be4b682 |
| Source note | uspto-grants-1991_11 |