HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 3-Bromo-2-chloropyridin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Chloropyridin-4-amine | HCID 84432 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-Bromo-2-chloropyridin-4-amine | HCID 29919300 | — |
Reaction Steps
4-Amino-2-chloropyridine (50 g, 388 mmol) was dissolved in glacial acetic acid (500 mL). To this solution was added NBS (75 g, 426 mmol) portionwise at RT (water bath cooling was provided to control the exothermicity). The reaction mixture was stirred at RT for 1 h at which point the reaction was found complete (as monitored by TLC). Solvent was removed under reduced pressure followed by azeotropic distillation with ethanol. The crude product was purified by column chromatography on silica gel (230-400 mesh) eluting with ethyl acetate hexane mixture.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07776857B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-6c3be5b444b84daba708f4d4a691daf9 |
| Source note | uspto-grants-2010_08 |