HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → N~3~-Benzylpyridine-2,3-diamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | 2,3-Diaminopyridine | HCID 9956 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | N~3~-Benzylpyridine-2,3-diamine | HCID 10397869 | — |
Reaction Steps
A mixture of 2,3-diaminopyridine (45 g), ethanol (500 ml), triethylamine (42 g) and benzyl bromide (70.5 g) was stirred at room temperature for 3 days. The solvent was evaporated in vacuo and the residue partitioned between chloroform (500 ml) and water (400 ml). The organic layer was eparated, filtered through a silica gel plug and evaporated in vacuo. The residue was triturated with hot chlorobutane to yield a brown powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04450164 |
| Source dataset | uspto-grants-1984_05 |
| ORD ID | ord-37275d50a019434292c0153254f8ffaa |
| Source note | uspto-grants-1984_05 |