HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 2,3,6-Trichloropyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Pentachloropyridine | HCID 16584 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,3,6-Trichloropyridine | HCID 23016 | — |
Reaction Steps
Collins et al., J. Chem. Soc., (c); pages 167-174 (1971) teach that halogens ortho and para to the ring nitrogen in pentachloropyridine are reactive with hydrazine hydrate. This reference further teaches the formation of tetrahalo-4-hydroxy pyridine from the action of aqueous sodium hydroxide on tetrahalo-4-hydrazino pyridines. From this same starting material, 2,3,6-trichloropyridine is formed from the reaction with cuprous oxide in hot water.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03971799 |
| Source dataset | uspto-grants-1976_07 |
| ORD ID | ord-68f3d21a828840e3aed137419e40e2b9 |
| Source note | uspto-grants-1976_07 |