HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Bromosuccinamide → 3-(benzyloxy)-5-bromo-1-(4-butylphenyl)pyridin-4(1H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Bromosuccinamide | HCID 9834204 | — |
| Reactant | 3-(benzyloxy)-1-(4-butylphenyl)pyridin-4(1H)-one | HCID 67419599 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-(benzyloxy)-5-bromo-1-(4-butylphenyl)pyridin-4(1H)-one | HCID 67419034 | — |
Reaction Steps
To a solution of 3-(benzyloxy)-1-(4-butylphenyl)pyridin-4(1H)-one (705 mg, 2.1 mmol) in AcOH (21 mL) was added N-bromosuccinamide (414 mg, 2.3 mmol) and the reaction mixture was stirred at room temperature. After 1 h, the mixture was concentrated under reduced pressure and purified by flash chromatography (50 g SiO2, 0-70% ethyl acetate/hexanes) to provide 3-(benzyloxy)-5-bromo-1-(4-butylphenyl)pyridin-4(1H)-one. LC/MS (M+H)+ 412/414.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09024032B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-bdc6f27d6a104e5d92a7e98d0c899522 |
| Source note | uspto-grants-2015_05 |