HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminopyridine → HCID 12875491, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminopyridine | HCID 1727 | — |
| Reactant | Bromodiphenylmethane | HCID 236603 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 12875491 | HCID 12875491 | — |
Reaction Steps
A mixture of 38 parts of 4-aminopyridine, 100 parts of bromodiphenylmethane and 500 parts by volume of acetonitrile is heated at reflux temperature for about three hours with stirring. The reaction mixture is filtered, the solid obtained washed with 125 parts by volume of hot acetonitrile and air-dried overnight at room temperature. The obtained solid is recrystallized from 500 parts by volume of ethanol to yield 4-amino-1-(diphenylmethyl)pyridinium bromide, as a colorless crystalline solid melting at about 260°-262° C. This compound has the following formula. ##STR19##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04267318 |
| Source dataset | uspto-grants-1981_05 |
| ORD ID | ord-ffc50efe4cf947c0afe3360fa558539f |
| Source note | uspto-grants-1981_05 |