HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 2-Amino-5-bromo-4-chloropyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Amino-4-chloropyridine | HCID 581866 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Amino-5-bromo-4-chloropyridine | HCID 44181812 | 80.3% |
Reaction Steps
To a solution of 2-amino-4-chloropyridine (0.50 g, 3.9 mmol) in acetonitrile (20 ml) was added dropwise a solution of N-bromosuccinimide (0.730 g, 4.1 mmol) in acetonitrile (10 ml). The reaction mixture was stirred at room temperature for 16 h then concentrated in vacuo. The crude product was purified by chromatography on silica gel (hexane/ethyl acetate 6:4) to give the title compound as a white solid (0.65 g, 80%); 1H-NMR (250 MHz, CDCl3) 6.63 (s, 1H) and 8.16 (s, 1H) (3-H, 6-H); LC-MS (ESI, m/z) Rt=4.8 min—206, 209 [(M+H+), BrCl isotopic pattern, 100%];
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08088761B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-1559f527f0384364acc53e9a8de53c79 |
| Source note | uspto-grants-2012_01 |