HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminopyridine → HCID 178419727, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Reactant | 4-Nitrobenzyl bromide | HCID 66011 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178419727 | HCID 178419727 | 88% |
Reaction Steps
1.04 g (11 mmol) of 2-aminopyridine and 2.39 g (11 mmol) of p-nitrobenzylbromide were dissolved in 20 mL CH3CN. The solution was warmed to reflux for 1 hr then cooled to room temperature, diluted with Et2O, and the solid filtered, washed 4× with Et2O and collected to yield 3 g (88%) of 1-(4-Nitro-benzyl)-1H-pyridin-2-ylidene-ammonium bromide (174) as an off white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08524756B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-cb8821ddff78456ab4920e185227b3dd |
| Source note | uspto-grants-2013_09 |